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This paper presents an experimental procedure for the characterization of the granitic rocks on a Mars-like environment. To gain a better understanding of the drilling conditions on Mars, the dynamic tensile behavior of the two granitic rocks was studied using the Brazilian disc test and a Split Hopkinson Pressure Bar. The room temperature tests were performed on the specimens, which had gone through thermal cycling between room temperature and - 70 degrees C for 0, 10, 15, and 20 cycles. In addition, the high strain rate Brazilian disc tests were carried out on the samples without the thermal cyclic loading at test temperatures of - 30 degrees C, - 50 degrees C, and - 70 degrees C. Microscopy results show that the rocks with different microstructures respond differently to cyclic thermal loading. However, decreasing the test temperature leads to an increasing in the tensile strength of both studied rocks, and the softening of the rocks is observed for both rocks as the temperature reaches - 70 degrees C. This paper presents a quantitative assessment of the effects of the thermal cyclic loading and temperature on the mechanical behavior of studied rocks in the Mars-like environment. The results of this work will bring new insight into the mechanical response of rock material in extreme environments.
Whereas stable homogenous states of aqueous hydrocarbon solutions are typically observed at high temperatures and pressures far beyond the critical values corresponding to individual components, the stability of such system may be preserved upon transition into the region of metastable states at low temperatures and low pressures. This work is dedicated to the study of the thermal stability of a water-methane mixture formed by cryogenic vapor phase deposition. The obtained thin films were studied using vibrational spectroscopy in the temperature range of 16-180 K. During thermal annealing of the samples, characteristic vibrational C-H modes of methane were monitored alongside the chamber pressure to register both structural changes and desorption of the film material. The obtained results reveal that upon the co-deposition of methane and water, methane molecules appear both in non-bound and trapped states. The observed broadening of the characteristic C-H stretching mode at 3010 cm(-1) upon an increase in temperature of the sample from 16 to 90 K, followed by narrowing of the peak as the temperature is reduced back to 16 K, indicates localization of methane molecules within the water matrix at lower temperatures.
We present a systematic study on the properties of Na(Y,Gd)F-4-based upconverting nanoparticles (UCNP) doped with 18% Yb3+, 2% Tm3+, and the influence of Gd3+ (10-50 mol% Gd3+). UCNP were synthesized via the solvothermal method and had a range of diameters within 13 and 50 nm. Structural and photophysical changes were monitored for the UCNP samples after a 24-month incubation period in dry phase and further redispersion. Structural characterization was performed by means of X-ray diffraction (XRD), transmission electron microscopy (TEM) as well as dynamic light scattering (DLS), and the upconversion luminescence (UCL) studies were executed at various temperatures (from 4 to 295 K) using time-resolved and steady-state spectroscopy. An increase in the hexagonal lattice phase with the increase of Gd3+ content was found, although the cubic phase was prevalent in most samples. The Tm3+-luminescence intensity as well as the Tm3+-luminescence decay times peaked at the Gd3+ concentration of 30 mol%. Although the general upconverting luminescence properties of the nanoparticles were preserved, the 24-month incubation period lead to irreversible agglomeration of the UCNP and changes in luminescence band ratios and lifetimes.