Temperature Interval Research Articles

Effect of long‐chain branching structures on supercritical CO2 foaming behavior of iPB‐1 with different crystalline form ratios

AbstractTo solve the poor cellular morphology of linear iPB‐1 during supercritical CO2 foaming, the modification and the special crystalline transition behavior of iPB‐1 were used to improve its foaming performance. Based on free radical polymerization, long‐chain branching iPB‐1 is achieved. Long‐chain branching structures not only reduce crystallinity of iPB‐1, but also increase the crystallization temperature. Long‐chain branching structures can accelerate the crystalline transformation rate of iPB‐1. After annealing at room temperature for 24 h, the crystalline transformation of the raw iPB‐1 material is completed by 14%, while long‐chain branching iPB‐1 reaches 33%. The crystalline transformation of the modified iPB‐1 is completed by 85% after annealing for 48 h. Compared with the raw iPB‐1 material with crystalline form I, the introduction of long‐chain branching structures is favorable for broadening the foaming temperature interval from 10 to 20°C, while the foaming temperature interval of the long‐chain branching iPB‐1 with crystalline form II increases to 25°C. The iPB‐1 with high content of crystalline form I and long‐chain branching structures are conductive to the formation of uniform cells. This will broaden the application of iPB‐1 foam in automotive interiors, packaging, and transportation fields.

A study of the interaction between volatile and char on the mechanism of NO and N2O conversion during nitrogen-containing biomass model (amino acids) combustion

The interaction between volatile and char is widespread in combustion. The effect of this interaction on the conversion of fuel-N to NOx is significant, but the mechanism remains to be comprehensively unveiled. Thus, in this paper, the NO and N2O conversion of nitrogen-containing biomass models (glutamate, glycine, phenylalanine) during combustion at high temperatures (800–1500 °C) is investigated using two combustion modes, separated combustion (in which volatile and char are burned separately) and coupled combustion (in which volatile and char are burned simultaneously), in an O2/Ar atmosphere. A new pathway for N2O formation resulting from the interaction between volatile and char is identified. At low temperatures, this interaction facilitates the conversion of fuel-N to N2O. For instance, during the separated combustion of glutamate at 800 °C, the conversion rates of fuel-N to N2O and NO are 26.3 % and 20.4 %, respectively. However, in coupled combustion, these conversion rates shift to 48.1 % for N2O and 3.6 % for NO. At high temperatures, this interaction promotes the conversion of fuel-N to NO. For instance, during the separated combustion and coupled combustion of glutamate at 1500 °C, the conversion rates of fuel-N to NO are 6.2 % and 16.6 %, respectively. Similar patterns are observed for the other two amino acids. In both combustion modes, the co-firing of cellulose, lignin, and hemicellulose with glutamic acid significantly suppresses the production of N2O. The conversion rate of N2O decreases by about 7 %–10 %, while the impact on NO release shows either a suppressive or promotive effect in different temperature intervals. These results play a crucial role in the development of efficient and clean combustion technology for biomass.

In vitro immune analysis of serum from the hemolymph of the anomuran crab Albunea symmysta (Linnaeus, 1758) displayed diversified reactions

The present investigation aims to substantiate that serum from the hemolymph of anomuran crab Albunea symmysta encompasses multiple immunological reactions in in vitro condition. The serum highly agglutinated human O erythrocytes in the presence of Ba2+. Distinct and unique sugar binding capacity of serum towards laminarin, N-acetyl sugars and higher binding specificity towards a glycoprotein, fetuin was inferred. In vitro enhancement of melanin synthesis due to enhanced oxidation of 3, 4-dihydroxy-dl-phenylalanine (dl-DOPA) by preincubation of nonself molecules with serum phenoloxidase (PO) was documented. Similarly, dl-DOPA oxidation by serum PO was reduced when preincubated with chemical inhibitors and copper chelators. Further, the crab serum lysed the vertebrate erythrocytes with maximum hemolysis against chicken and it unveiled dependency on divalent cation, serum concentration, ionic strength, pH, temperature and time interval. Occurrence of maximum hemolysis at a concentration of 30 µl, pH 8.0, temperature 37 °C and time interval of 60 min in the presence of Ba2+ were documented. Interestingly, serum hemolysis was reduced by different osmoprotectants suggesting a colloid-osmotic mechanism involving in hemolysis. It was observed that A. symmysta serum had antimicrobial activity against Gram-positive Staphylococcus aureus and fungal pathogen Candida albicans. The serum showed higher glycan content, potent lysozyme and free radical scavenging activity suggesting the existence of potential immune molecules of therapeutic use. These results clearly demonstrated the diversified immunogenicity of A. symmysta serum confirming a highly conserved non-specific immunity of crustaceans

Measurement setup for Nernst and Seebeck effect at high temperatures and magnetic fields tested on elemental bismuth and full-Heusler compounds.

In this work, a measurement setup to study the Seebeck and Nernst effect at high temperatures and high magnetic fields is introduced and discussed. The measurement system allows for simultaneous measurements of both thermoelectric effects up to 700K and magnetic fields up to 12T. Based on theoretical concepts, measurement equations are derived that counteract constant spurious offset voltages and, therefore, inhibit systematic errors in the measurement setup. The functionality is demonstrated on polycrystalline samples of elemental bismuth as well as various full-Heusler materials, exhibiting an anomalous Nernst effect. In all samples, the measured Seebeck and Nernst coefficients align excellently with the reported values. This allows future research to substantially extend the measured temperature and field intervals, commonly limited to temperatures below room temperature. For the first time, the thermoelectric and thermomagnetic properties of these materials are reported up to temperatures of 560K.

Phase transformation and strengthening of the gas-atomized FeCoCrNiMo0.5Al1.3 high-entropy alloy powder during annealing

Phase evolution and strengthening of the FeNiCoCrMo0.5Al1.3 powder alloy produced via inert gas atomization and annealed in the temperature interval of 300–800 °C have been studied by X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy, and microhardness testing. It was found that annealing at 300–600 °C leads to an increase of the element segregations between the several solid solutions with a rise of the lattice misfit (ε) to 1.5 % and microhardness growth to 1070 HV. It was assumed that elastic stress caused by the element partitioning is the main strengthening mechanism: microhardness rises linearly with misfit rise with dHV/dε = 43400 MPa. Sigma arises after the maximum elastic deformation (in 1.5 %) was reached. Formation of the dispersed coherent sigma phase in the annealing interval 600–800 °C results in the microhardness rise. Oxidation that began at 800 °C in 27 h is accompanied with FCC formation due to a depletion of the B2 in Al caused by Al2O3 formation. Estimation of the activation energy of the initial stage of the solid solution decomposition gives a very low value in 0.65eV, apparently caused by the high concentration of quenched vacancies. The activation energy of sigma formation approximately coincides with the activation energy of self-diffusion in BCC metals (about 2.60 eV).

Effect of oxidation temperature on physical properties of polycrystalline β-Ga2O3 grown by thermal oxidation of GaN in O2 ambient from 900 to 1400 °C

This study aimed to investigate the effect of oxidation temperature on the physical properties of β-Ga2O3 grown by thermal oxidation of GaN in the O2 ambient at high oxidation temperatures from 900 to 1400 °C. Notably, the analysis of the oxidation temperatures ranging from 1100 to 1400 °C remains unexplored in the other studies. The effects of the oxidation temperature on the physical properties were investigated via X-ray diffraction, X-ray photoelectron spectroscopy, and field-emission scanning electron microscopy (FESEM). At all oxidation temperatures, XPS results revealed oxygen deficiency. The top FESEM images indicated disordered nanocolumn structures on the surface of the oxide layer, which increased in abundance with oxidation temperatures exceeding 1100 °C. Energy-filtered high-resolution transmission electron microscopy images and the selected area electron diffraction patterns revealed that the top nanocolumns and the oxidized layer comprised polycrystalline β-Ga2O3. Additionally, the cross-sectional lamellae prepared through focused ion beam milling revealed an increase in the thickness of the β-Ga2O3 layer with oxidation temperature. To account for the variations in the oxide layer thickness, the oxidation temperatures were classified into two ranges of 900–1100 °C and 1100–1400 °C for calculating the activation energy. Moreover, this study assumed that the activation energy required for the oxidation process remained constant within each temperature interval. According to Arrhenius's model, the activation energy from 900 to 1100 °C was calculated to be 286.15 kJ/mol (2.97 eV). Furthermore, the activation energy from 1100 to 1400 °C was determined to be 111.33 kJ/mol (1.15 eV).

Description of CuInP<sub>2</sub>S<sub>6</sub> ferrielectrics in a mixed Ising model

The appearance of spontaneous polarization in CuInP2S6 ferrielectrics is related to the second order Jahn-Teller effect for copper cations located in a double-well local potential, the stereoactivity of indium cations located in a three-well local potential, as well as the valence fluctuations of phosphorus cations. The paraelectric to ferrielectric phase transition is primarily determined by the coupling of indium cations with their surroundings. This transition can be analyzed using the mixed Ising model with spins s = 1/2 and S = 1. The spectrum of pseudospin fluctuations at different temperatures was calculated using a mean-field approach for a set of quantum anharmonic oscillators. The results were then compared with Raman spectroscopy data for CuInP2S6 crystal. The analysis indicates that the lattice anharmonicity below 150 K, is mainly determined by the indium sublattice, leading to the coexistence of the glassy state and ferrielectric phase. Above 150 K, the anharmonicity of the copper sublattice activates the ionic conductivity and results in the existence of a long-ranged fluctuated cluster of spontaneous polarization in a temperature interval of the paraelectric phase above TC.

Supramolecular Interaction Modulation in Thermosensitive Composites: Enantiomeric Recognition and Chiral Site Regeneration.

Herein, a novel strategy was implemented to modulate the supramolecular interaction between enantiomers and chiral recognition sites (CRSs), effectively resolving the issue of CRS saturation. Randomly methylated-β-cyclodextrin (Rm-β-CD) was used as the CRS (host molecule), and polymerized ionic liquids [poly([vbim]TFSI)] were used as the supramolecular modulator (guest molecule), which self-assembled to generate thermosensitive supramolecular host/guest complexes. The enantiomeric binding capacity and enantioselectivity of chiral separation systems centered on supramolecular host-guest complexes are characterized by a high degree of temperature dependence. Poly([vbim]TFSI) bonded to Rm-β-CD at temperatures between 17 °C ± 3 and 50 °C ± 3 °C, and the binding free energy difference (|ΔΔG|) between the (S)- and (R)-enantiomer was 0.55. Conversely, poly([vbim]TFSI detached from Rm-β-CD at temperatures >50 °C ± 3 °C or <17 °C ± 3 °C, and |ΔΔG| between (S)- and (R)-enantiomer was 0.03. The |ΔΔG| value of the (R)-enantiomer can reach 0.86 in two temperature intervals. Therefore, the binding of poly([vbim]TFSI) to Rm-β-CD afforded the favorable separation of four racemic sample mixtures: mandelic acid (e.e.% = 61.3%), ibuprofen (e.e.% = 21.6%), warfarin (e.e.% = 14.9%), and naproxen (e.e% = 18.2%). The detachment of poly([vbim]TFSI) from Rm-β-CD released the enantiomer bound to CRSs. The decomplexation of mandelic acid reached 75.1%.

Performance characterization and microscopic properties of asphalt modified with rapeseed heavy oil-activated waste rubber powder

To improve the waste rubber powder modified asphalt viscosity is high, poor storage stability, and other shortcomings, 40 mesh, 60 mesh, and 80 mesh are three kinds of mesh rubber powder using rapeseed heavy oil pre-swelling activation way to prepare modified asphalt, improve the waste rubber powder modified asphalt storage stability and reduce the viscosity. The optimum blending amount of rapeseed heavy oil-activated waste rubber powder was determined by setting three oil-rubber ratios, and the unactivated waste gum powder modified asphalt was set as a control group, and the physical, rheological, and microscopic properties of the asphalt were evaluated accordingly. The optimum preparation parameters under the premise of setting the total dosage of modifier as 20% were: the mass ratio of rubber powder to rapeseed oil was 2:1, and the mesh size of rubber powder was 80 mesh. Rapeseed heavy oil-activated waste rubber powder modified asphalt storage stability and low-temperature performance improved, viscosity decreased, but high-temperature performance decreased at the same time. Compared with the unactivated waste rubber powder modified asphalt, the softening point decreased by an average of 16%, the needle penetration increased by an average of 19%, the ductility increased by an average of 44%, the viscosity decreased by an average of 22%, and the softening point difference decreased by an average of 44%. In the high-temperature rheological performance test set temperature interval, the rutting coefficient G*/sinδ decline, creep stiffness Ѕ, and creep rate m have increased. Therefore, rapeseed heavy oil activation can effectively improve the overall stability of waste rubber powder-modified asphalt and can reduce the overall viscosity, which is conducive to the uniform dispersion of rubber powder in asphalt.

A newly developed model for estimating snow depth in ungauged areas

The presence of snow significantly affects the hydrological cycle and soil moisture globally. Nowadays, with the expansion of science, different satellites can measure snow depth all over the world. By establishing a conditional relationship between mean temperature and the Proportion of Snowfall to Total Precipitation (PSTP), this study proposes a method for snow depth estimation for ungauged stations. The case study of this research is Iran. Most of Iran's climate is arid due to its location in the Middle East, making it one of the countries with the lowest rainfall worldwide. On the other hand, this country enormously depends on water resources. Consequently, an accurate and valid estimate of snow amounts in Iran is essential. To reach this goal, we analyzed daily data from 12 synoptic and climatological stations between 1970 and 2020, including rainfall, snow depth, and mean temperature. For each station, the PSTP at 0.5 °C air temperature intervals was determined and fitted to a double sigmoid model that allows snow depth estimation. The evaluation of the snow depth approximated by the double sigmoid model was done using R2, RRMSE, EF, and Bias statistics against the observational data. R2 values in the Era-5 dataset in all stations are lower than 0.5. Additionally, it should be noted that in certain stations, the bias values surpass 20 mm. Furthermore, in 75 percent of the stations, the RRMSE values exceed 0.6. By utilizing the DSBE model, it is possible to achieve a reduction of 122.4 and 0.7 in Bias and RRMSE values, respectively. The R2 between observed and estimated snow depth was estimated between 0.81 and 1 in ten of the studied stations and 0.65 and 0.8 in the other two stations. Moreover, the findings imply that the proposed model is a suitable technique for estimating snow depth in remote areas lacking snowfall measurement.

Low temperature vaporisation of Cr from fluoride flux reacted at 1350 °C with Al–Cr–Fe powder: Thermochemical analysis of gas phase reactions and nano-strand formation

The submerged arc welding (SAW) process is complex because multi-phase reactions occur simultaneously across a large temperature interval from 2500 °C in the arc cavity, down to the weld pool liquidus temperare at the slag-weld pool interface. This complexity hinders research on specific process metallurgy aspects, such as gas formation from the oxy-fluoride slag. The main objective of this work is to illustrate a low temperature experimental technique as an accurate reaction simulation experiment of SAW flux oxy-fluoride slag behaviour in terms of gas formation and metal powder assimilation reaction mechanisms as observed in the SAW process. The oxy-fluoride slag behaviour was confirmed by identification and analyses of nano-strand formation in the reacted slag formed from the reaction of welding flux with Al-Fe-Cr metal powders at 1350 °C. The observed nano-strand formation agrees with similar observations in SAW post-weld slags used to confirm of oxy-fluoride vaporisation and re-condensation. Element distribution from energy dispersive X-ray spectroscopy (EDS) maps and thermochemical calculations were used to gain insights into the reactions in nano-strand formation. The nano-strands contained chromium patches and spots of less than 1 μm in scale, confirming that added Cr metal powder assimilated via the gas phase. Cr-fluoride formed part of the oxy-fluoride slag and likely formed Cr-fluoride gas. Cr was recovered via re-condensation of Cr vapour formed from the reaction of Cr-fluoride with Al gas. This work presents an accurate low temperature simulation method of gas formation and metal powder assimilation reactions in oxy-fluoride slags as in the SAW process.

Simulation and experimental study of temperature and mass distributions of indium metal in vacuum evaporation

The temperature field and spatial distribution of metal vapor (i.e., flow field) are critical for the purity and direct yield of metals. However, it is impossible to accurately determine the temperature field and distribution of the metal vapor in a vacuum furnace. This study developed a surface-to-surface thermal radiation and volume of fluid multiphase flow coupling model. The temperature distribution and mass distribution of indium vapor in the vertical vacuum furnace at different temperatures from 1423 to 1573 K under the condition of 1 Pa were obtained. The reliability of the model was verified by experimental data obtained under the same conditions as the simulation. The temperature difference between the inside and outside of the condensing plate was 30–45 K in the temperature interval of 1423–1573 K. The temperature difference between the inside wall and the center of the condensing plate was 10 K. The simulation results of indium vapor mass distribution match with the experimental values; the overall temperature error is 5%, and the volatility error is less than 15%. The model developed in this study can be used to predict the temperature field and metal vapor distribution in a vacuum furnace, which will significantly reduce experimental exploration and accurately guide the production practice of vacuum metallurgy. This will expand the application of vacuum metallurgy technology in metal purification, material preparation, waste recycling, and other industries. This can effectively reduce exploratory experiments in the process of vacuum distillation to prepare high-purity metals, reduce the consumption of resources and energy in the experiment and production process, and achieve clean production.

Copper-Enriched Nanostructured Conductive Thermoelectric Copper(I) Iodide Films Obtained by Chemical Solution Deposition on Flexible Substrates

The objects of our research are flexible thin-film thermoelectric materials with nanostructured CuI layers 0.5–1.0 μm thick, fabricated by the chemical solution method Successive Ionic Layer Adsorption and Reaction (SILAR) on flexible polyethylene terephthalate and polyimide substrates. These cubic γ-CuI films differ from films obtained by other chemical solution methods, such as spin-coating, sputtering, and inject printing, in their low resistivity due to acceptor impurities of sulfur and oxygen introduced into CuI from aqueous precursor solutions during SILAR deposition. Energy barriers at the boundaries of 18–22 nm CuI nanograins and a large number of charge carriers inside the nanograins determine the transport properties in the temperature interval 295–340 K characterized by transitions from semiconductor to metallic behavior with increasing temperature, which are typical of nanostructured degenerate semiconductors. Due to the resistivity of about 0.8 mΩ· m at 310 K and the Seebeck coefficient 101 μV/K, the thermoelectric power factor of the CuI film 1.0 μm thick on the polyimide substrate is 12.3 μW/(m · K2), which corresponds to modern thin-film p-type thermoelectric materials. It confirms the suitability of CuI films obtained by the SILAR method for the fabrication of promising inexpensive non-toxic flexible thermoelectric materials.

A Study on the Pyrolysis Behavior and Product Evolution of Typical Wood Biomass to Hydrogen-Rich Gas Catalyzed by the Ni-Fe/HZSM-5 Catalyst

The thermo-chemical conversion of biomass wastes is a practical approach for the value-added reclamation of bioenergy in large quantities, and pyrolysis plays a core role in this process. In this work, poplar (PR) and cedar (CR) were used as staple wood biomasses to investigate the apparent kinetics of TG/DTG at different heating rates. Secondly, miscellaneous wood chips (MWC), in which PR and CR were mixed in equal proportion, were subjected to comprehensive investigations on their pyrolysis behavior and product evolution in a fixed bed reactor with pyrolysis temperature, catalyst, and the flow rate H2O steam as influencing factors. The results demonstrated that both PR and CR underwent three consecutive pyrolysis stages, the TG/DTG curves shifted to higher temperatures, and the peak temperature intervals also enhanced as the heating rate increased. The kinetic compensation effect expression and apparent reaction kinetic model of CR and PR pyrolysis were obtained based on the law of mass action and the Arrhenius equation; the reaction kinetic parameter averages of Ea and A of its were almost the same, which were about 72.38 kJ/mol and 72.36 kJ/mol and 1147.11 min−1 and 1144.39 min−1, respectively. The high temperature was beneficial for the promotion of the pyrolysis of biomass, increased pyrolysis gas yield, and reduced tar yield. This process was strengthened in the presence of the catalyst, thus significantly increasing the yield of hydrogen-rich gas to 117.9 mL/g-biomass. It was observed that H2O steam was the most effective activator for providing a hydrogen source for the whole reaction process, promoted the reaction to proceed in the opposite direction of H2O steam participation, and was beneficial to the production of H2 and other hydrocarbons. In particular, when the flow rate of H2O steam was 1 mL/min, the gas yield and hydrogen conversion were 76.94% and 15.90%, and the H2/CO was 2.07. The yields of H2, CO, and CO2 in the gas formation were significantly increased to 107.35 mL/g-biomass, 53.70 mL/g-biomass, and 99.31 mL/g-biomass, respectively. Therefore, H2 was the most dominant species among gas products, followed by C-O bond-containing species, which provides a method for the production of hydrogen-rich gas and also provides ideas for compensating or partially replacing the fossil raw material for hydrogen production.

The Inhibition Action of Some Brij-Type Nonionic Surfactants on the Corrosion of OLC 45 in Various Aggressive Environments.

The corrosion protection property of three Brij-type surfactants, namely, Brij 35, Brij 56 and Brij 58P, was considered on OLC 45 carbon steel in a 0.5 M H2SO4 medium. The efficacy for these organic compounds was examined using potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) methods, scanning electron microscopy (SEM) procedures, and Fourier transform infrared (FT-IR) spectroscopy. We hypothesized that these surfactants hinder the corrosion for OLC 45 samples through a protecting mechanism owing to the adsorption of organic molecules that form an inhibitive film or through the formation of complex oxides. These surfactants exhibited an appreciable protective effect against OLC 45 corrosion, operating as mixed inhibitors, as could be demonstrated by their influence on the electrochemical characteristics of the metallic substrates. The adsorption of surfactants over the substrates zone conformed to the representation of the Langmuir isotherm. The effect of temperature on the electrochemical comportment of the OLC 45 specimens in H2SO4 without and with Brij at 800 ppm was examined in the temperature interval of 293 to 333 K. The negative estimate of thermodynamic attributed as Gibbs free energy of adsorption presented the spontaneity of the adsorption activity. The investigation with FT-IR and SEM established the adsorption of Brij and the constitution of the corrosive components on the OLC 45 surface. Electrochemical determinations of these surfactants indicated its anticorrosion inhibition performance and the highest inhibition of 96% was reached when the Brij 35 concentration was at 800 or 1000 ppm, while for Brij 56 and Brij 58P, the highest inhibition was obtained when their concentrations were 500, 800, or 1000 ppm.

Study of the properties of combined multilayer polymer materials for aeronautical equipment

The results of studies of changes in the physical and mechanical properties of heat-resistant polyethylene terephthalate (PET), polymide (PI) and fluoroplastic (PP) films, as well as synthetic polyethylene terephthalate (PET) and aramid fabrics in a wide range of specified exposure temperatures and temperature exposure times are presented. The most suitable heat-resistant polymer films and fabrics for use in inflatable structures of aeronautical equipment have been identified. An assessment of the operational parameters of the investigated materials showed linear character of change in properties in a given temperature and time interval of researches.

Self-contained calibration samples and measurements of the thermoelectric figure of merit: A method to improve accuracy

Despite more than seven decades of active research and development in thermoelectricity, the accurate measurement of the thermoelectric (TE) properties of bulk materials has remained a challenge, mainly because of the strong interrelation between thermal and electrical phenomena. This work highlights practical advancements in methods and instrumentation dedicated to the simultaneous measurements of TE properties such as the Seebeck coefficient (S), the thermal (κ), and electrical (σ) conductivities and the dimensionless TE figure of merit ZT = S2σT/κ. The accuracy of a Harman based approach, as implemented by the ZT-Scanner (TEMTE Inc.), applicable to the simultaneous measurement of the above TE properties, has been made possible by a self-contained calibration procedure, which is based on the availability of two samples of the same homogeneous material having different shape factors. It is of practical importance that this approach provides a simple procedure to obtain the calibration for the figure of merit ZT and the thermal conductivity in the temperature interval from 300 to 720 K. In addition, we show that a simplified Harman setup with no thermocouples attached to the sample can also be used for self-contained calibrated ZT measurements. It is concluded that the implemented steady-state approach decreases the relative error down to 1%–2% for ZT measurements and can be recommended for most applications not involving dynamical behavior. In particular, it is proposed that self-generated calibration samples can critically increase the quality and ease of comparison of TE measurements if they are adopted by the TE community.

Dehydration kinetics of nanoconfined water in beryl probed by high temperature single crystal synchrotron X-ray diffraction

Understanding changes in material properties through external stimuli plays a key role in validating the expected performance of materials and engineering material properties in a controlled manner. Here, we introduce a fundamental protocol to deduce dehydration reactions kinetics of water confined in nanopore channels, with the cyclosilicate beryl as the scaffold of interest, using time-resolved synchrotron X-ray diffraction (SXRD), in the temperature interval of 298–1038 K. The temperature-dependent intensity (I)\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$(I)$$\\end{document} of the strongest reflection (112) was used as the crystallite variable. An estimation of an isobaric thermal crystallite coefficient, k\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$k$$\\end{document}, analogous with the isobaric thermal expansion coefficient, established the rate of relative crystallization as a function of temperature, ∂I∂T\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\frac{\\partial I}{\\partial T}$$\\end{document}. A plot of lnk\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$lnk$$\\end{document} and 1T\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\frac{1}{T}$$\\end{document} gives rise to two kinetic steps, indicating a slow dehydration stage up to ~ 700 K and a fast dehydration stage up to the investigated temperature 1038 K. The crystal structure of beryl determined up to 1038 K, in temperature increment as small as 10 K, indicates the presence of channel ions Na and Fe and a gradual decrease of water upon heating.

Theoretical evaluation of the impact of diverse treatment conditions by calculation of the tumor control probability (TCP) of simulated cervical cancer Hyperthermia-Radiotherapy (HT-RT) treatments in-silico

Introduction Hyperthermia (HT) induces various cellular biological processes, such as repair impairment and direct HT cell killing. In this context, in-silico biophysical models that translate deviations in the treatment conditions into clinical outcome variations may be used to study the extent of such processes and their influence on combined hyperthermia plus radiotherapy (HT + RT) treatments under varying conditions. Methods An extended linear-quadratic model calibrated for SiHa and HeLa cell lines (cervical cancer) was used to theoretically study the impact of varying HT treatment conditions on radiosensitization and direct HT cell killing effect. Simulated patients were generated to compute the Tumor Control Probability (TCP) under different HT conditions (number of HT sessions, temperature and time interval), which were randomly selected within margins based on reported patient data. Results Under the studied conditions, model-based simulations suggested a treatment improvement with a total CEM43 thermal dose of approximately 10 min. Additionally, for a given thermal dose, TCP increased with the number of HT sessions. Furthermore, in the simulations, we showed that the TCP dependence on the temperature/time interval is more correlated with the mean value than with the minimum/maximum value and that comparing the treatment outcome with the mean temperature can be an excellent strategy for studying the time interval effect. Conclusion The use of thermoradiobiological models allows us to theoretically study the impact of varying thermal conditions on HT + RT treatment outcomes. This approach can be used to optimize HT treatments, design clinical trials, and interpret patient data.

Study of hydrogen sorption and desorption processes of zirconium beryllide ZrBe2

One of the promising intermetallic compounds for use in nuclear and fusion reactors, as well as in hydrogen energy technology, are intermetallic compounds of beryllium with metals such as Ti, V, Zr and Nb. Beryllium-based intermetallics are not only a promising material for blankets of future fusion reactors, but can also be utilized in other areas of the nuclear industry, including fission reactor reflectors, rocket and space technology. The interest in studies of the interaction of hydrogen isotopes with beryllides is related to the accumulation of tritium and helium in the material, formed as a result of nuclear reactions under neutron irradiation, and is caused by the need for understanding the processes arising from such interaction.In this work, hydrogen sorption and desorption processes of zirconium beryllide ZrBe2 produced by industrial technologies at JSC “Ulba Metallurgical Plant” (JSC UMP) were investigated. The experiments were performed by the Sievert’s and thermal desorption spectrometry (TDS) methods. In TDS experiments deuterium was chosen for samples saturation to reduce the possible error in determining fluxes associated with the release of hydrogen from the elements of the vacuum chamber.An equation for hydrogen solubility in zirconium beryllide ZrBe2 was obtained by processing the experimental data obtained by the Sievert’s method:S=0.46±0.1molm3∙Pa12∙exp-13.3±0.5kJmolRTThe temperature intervals of formation and decomposition of two different hydride phases (deuterides) of zirconium beryllide ZrBe2 at ∼ 600 K and ∼ 900 K have been established in TDS experiments.