Frequency aspects of the THz photomixer

In the paper methods of the terahertz photomixer operational frequency estimation are considered. Three methods are investigated — estimation of the frequency via direct measurements of the laser heterodyne compounds, via calculations from datasheets, and via calculations from raw collected data obtained from the photomixer system.     

The Tucson-Melbourne three-nucleon force in the automatized partial-wave decomposition

A recently developed procedure for a partial-wave decomposition of a three-nucleon force is applied to the p \pi -p \pi , p \pi -r \rho and r \rho -r \rho components of the Tucson-Melbourne three-nucleon potential. The resulting matrix elements for the p \pi -p \pi and p \pi -r \rho components are compared with the values obtained using the standard approach to the partial-wave decomposition, in which the p \pi -r \rho expressions for the matrix elements are also derived and presented. Several numerical tests and results for the triton binding energy and the correlation function prove the reliability and efficiency of the new method.     

Effect of Protic Ionic Liquid and Surfactant Structure on Partitioning of Polyoxyethylene Non‐ionic Surfactants

The partitioning constants and Gibbs free energies of transfer of poly(oxyethylene) n‐alkyl ethers between dodecane and the protic ionic liquids (ILs) ethylammonium nitrate (EAN) and propylammonium nitrate (PAN) are determined. EAN and PAN have a sponge‐like nanostructure that consists of interpenetrating charged and apolar domains. This study reveals that the ILs solvate the hydrophobic and hydrophilic parts of the amphiphiles differently. The ethoxy groups are dissolved in the polar region of both ILs by means of hydrogen bonds. The environment is remarkably water‐like and, as in water, the solubility of the ethoxy groups in EAN decreases on warming, which underscores the critical role of the IL hydrogen‐bond network for solubility. In contrast, amphiphile alkyl chains are not preferentially solvated by the charged or uncharged regions of the ILs. Rather, they experience an average IL composition and, as a result, partitioning from dodecane into the IL increases as the cation alkyl chain is lengthened from ethyl to propyl, because the IL apolar volume fraction increases. Together, these results show that surfactant dissolution in ILs is related to structural compatibility between the head or tail group and the IL nanostructure. Thus, these partitioning studies reveal parameters for the effective molecular design of surfactants in ILs.     

The Intensity of Heat Exchange between Rock and Flowing Gas in Terms of Gas-Geodynamic Phenomena

Gas-induced geodynamic phenomena can occur during underground mining operations if the porous structure of the rock is filled with gas at high pressure. In such cases, the original compact rock structure disintegrates into grains of small dimensions, which are then transported along the mine working space. Such geodynamic events, particularly outbursts of gas and rock, pose a danger both to the life of miners and to the functioning of the mine infrastructure. These incidents are rare in copper ore mining, but they have recently begun to occur, and have not yet been fully investigated. To ensure the safety of mining operations, it is necessary to determine parameters of the rock–gas system for which the energy of the gas will be smaller than the work required to disintegrate and transport the rock. Such a comparison is referred to as an energy balance and serves as a starting point for all engineering analyses. During mining operations, the equilibrium of the rock–gas system is disturbed, and the rapid destruction of the rock is initiated together with sudden decompression of the gas contained in its porous structure. The disintegrated rock is then transported along the mine working space in a stream of released gas. Estimation of the energy of the gas requires investigation of the type of thermodynamic transformation involved in the process. In this case, adiabatic transformation would mean that the gas, cooled in the course of decompression, remains at a temperature significantly lower than that of the surrounding rocks throughout the process. However, if we assume that the transformation is isothermal, then the cooled gas will heat up to the original temperature of the rock in a very short time (<1 s). Because the quantity of energy in the case of isothermal transformation is almost three times as high as in the adiabatic case, obtaining the correct energy balance for gas-induced geodynamic phenomena requires detailed analysis of this question. For this purpose, a unique experimental study was carried out to determine the time required for heat exchange in conditions of very rapid flows of gas around rock grains of different sizes. Numerical simulations reproducing the experiments were also designed. The results of the experiment and the simulation were in good agreement, indicating a very fast rate of heat exchange. Taking account of the parameters of the experiment, the thermodynamic transformation may be considered to be close to isothermal.     

Epitaxial graphene perfection vs. SiC substrate quality

Polytype instability of SiC epitaxial films was the main focus of attention in the experiment performed since this factor has a decisive influence on graphene growth, which was the second stage of the experiment. Layers deposited in various initial C/Si ratios were analyzed.     

Calculations of Three-Nucleon Reactions

Faddeev calculations using the chiral three-nucleon force in next-to-next-to-next-to-leading-order show that this force is too weak to provide an explanation for the low-energy A _y puzzle. The large discrepancy between data and theory for the neutron–neutron quasi-free-scattering cross section in low energy neutron–deuteron breakup requires a modification of the ${^{1}S_0}$ neutron–neutron force. We discuss the consequences that a bound ${^{1}S_0}$ state of two neutrons has on neutron–deuteron scattering observables. At higher energies we compare the solutions of the non-relativistic three-nucleon Faddeev equations with three-nucleon force included to the solutions of its Poincaré invariant version.     

Vibrational Properties of LaNb0.8M0.2O4-δ (M=As,Sb, V,and Ta)

LaNb_0.8M_0.2O_4-δ (where M=As, Sb, V, and Ta) oxides with pentavalent elements of different ionic sizes were synthesized by a solid-state reaction method. The vibrational properties of these oxides have been investigated. These studies revealed that the substituent element influences both Debye temperature value as well as the Raman active vibrational modes. Additionally, the low-temperature vibrational properties of LaNb_0.8Sb_0.2O_4-δ have been determined to show the phase transition occurrence at 260 K which is lower than previously reported.     

NHC-Rhodium-Catalyzed Synthesis of Novel Silsesquioxanes Containing S-Si and S-Ge Bonds and Their Application in Hydrosilylation Process

The efficient and straightforward NHC-rhodium-catalyzed thiol-silane and thiol-germanane coupling reactions, leading to new classes of functionalized SQ-based materials, are presented for the first time. The proposed strategies use commercially available reagents and show a broad functional groups tolerance, which opens a possibility of effective synthetic procedures of biologically active compounds.