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One of the long-standing challenges in experimental physics is the observation of room-temperature superconductivity . Recently, high-temperature conventional superconductivity in hydrogen-rich materials has been reported in several systems under high pressure . An  important discovery leading to room-temperature superconductivity is the pressure-driven disproportionation of hydrogen sulfide (H S) to H S, with a confirmed transition temperature of 203 kelvin at 155 gigapascals . Both H S and CH readily mix with hydrogen to form guest-host structures at lower pressures , and are of  comparable size at 4 gigapascals. By introducing methane at low pressures into the H S + H precursor mixture for H S, molecular exchange is allowed within a large assemblage of van der Waals solids that are hydrogen-rich with H inclusions; these guest-host structures become the building blocks of superconducting compounds at extreme conditions. Here we report superconductivity in a photochemically transformed carbonaceous sulfur hydride system, starting from elemental precursors, with a maximum superconducting transition temperature of 287.7 ± 1.2 kelvin (about 15 degrees Celsius) achieved at 267 ± 10 gigapascals. The superconducting state is observed over a broad pressure range in the diamond anvil cell, from 140 to 275 gigapascals, with a sharp upturn in transition temperature above 220 gigapascals. Superconductivity is established by the observation of zero resistance, a magnetic susceptibility of up to 190 gigapascals, and reduction of the transition temperature under an external magnetic field of up to 9 tesla, with an upper critical magnetic field of about 62 tesla according to the Ginzburg-Landau model at zero temperature. The light, quantum nature of hydrogen limits the structural and stoichiometric determination of the system by X-ray scattering techniques, but Raman spectroscopy is used to probe the chemical and structural transformations before metallization. The introduction of chemical tuning within our ternary system could enable the preservation of the properties of room-temperature superconductivity at lower pressures.

The interaction of the polyphenol–protein–polysaccharide ternary system plays a critical regulatory role in many biological processes including cellular signal transduction, molecular recognition, and assembly. Moreover, the interactions of the three elements can form complex molecular structures and affect their respective functions and activities. It is necessary to clarify the correlation between the binding force and functional characteristics of polyphenols, proteins, and polysaccharides in the ternary system to effectively improve the sensory, functional, and nutritional properties of food. Hence, this paper systematically reviews the interactions of the ternary system composed of polyphenols, proteins, and polysaccharides. Moreover, this article also analyzes the interaction between the two components in the ternary system based on the functional characteristics of these components. Furthermore, this review comprehensively introduces the application of ternary systems. The findings are expected to provide important guidance for the polyphenol–protein–polysaccharide ternary system in biology, medicine, and food industry.

The electrochemical response and corrosion associated with the Q-phase (Al sub( x)Cu sub( y)Mg sub( z)Si sub( w)) intermetallic compound was studied. Q-phase intermetallics are the principal strengthening phase in a number of Cu-containing 6xxx series (Al-Mg-Si) alloys, and Q-phase has not previously been uniquely studied in regard to its influence on localized corrosion in detail. Herein, quasi in situ scanning transmission electron microscopy was utilized in understanding the localized corrosion response associated with nanoscale Q-phase precipitates in a Cu-containing 6xxx series Al alloy sheet with a composition (in wt%): 97.3Al-0.9Si-0.74Mg-0.84Cu-0.08Fe-0.14Mn. Furthermore, the Q-phase compound was also produced on the microscale within a bulk-synthesized alloy. The electrochemical behavior of the microscale Q-phase was studied using a micro-electrochemical capillary cell and by potentiodynamic polarization. Quasi in situ scanning electron microscopy was also performed on the bulk alloy synthesized to contain microscale Q-phase, revealing that Q-phase was comparatively noble relative to the matrix and other intermetallic phases present-even following extended immersion in 0.1 M NaCl. The work herein also indicates that Q-phase undergoes incongruent dissolution/dealloying, with fine nanoscale Cu particles, containing multiple twins, were observed upon Q-phase following a period of corrosion.

Coupling the glycerol oxidation and hydrogen evolution reactions can significantly reduce the energy consumption of the electrolytic water hydrogen production system, achieve hydrogen production while preparing high value-added chemicals at a lower cost, and greatly improve the economic value of the entire hydrogen production system. In this work, CoMoP ternary nanocomposite has been successfully decorated onto the surface of 304 stainless steel mesh. The surface decoration with CoMoP ternary ionics nanocomposite greatly enhances the electron transfer in the catalytic system. The optimized catalyst exhibits a high activity for electrocatalytic glycerol oxidation coupling with alkaline hydrogen evolution reaction. A hydrogen-producing electrolysis cell with a formate faradaic efficiency of 60 % has been assembled, which can achieve a decomposition voltage as low as 1.60 V at a current density of 10 mA cm -2 . More importantly, the respective roles of the three chemical elements in the CoMoP ternary composite electrocatalyst have been thoroughly studied by DFT. This study provides scientific insight into developing future ternary systems for electrocatalysis.

Methyl Tertiary Butyl Ether (MTBE) and Methanol are effective fuel oxygenate that boost octane number, improve fuel performance, combustion behavior and minimize environmental pollutant emissions. In the petroleum business, however, their high-water solubility restricts their use in terms of fuel homogeneity loss. This work presents a full investigation map for the status of the phase diagram for the tertiary system of MTBE-methanol-water at different temperatures; 0, 40, and 70oC, and different pressures; 1.0 and 3.0 atm, based on different compositions. Furthermore, the thermodynamic coefficient, UNIFAC-LL, was linked to the Aspen plus Version 9. After validation of the software by the real experimental data, the software was used to complete the full map at all missing conditions. Pressure does not influence the occurrence of phase transitions, but the temperature has a minor effect on the LLE. The methanol concentration at which phase separation occurred dropped from 43% to 31.2% when the temperature was lowered from 70 to 40°C. With the use of simulation, the compositions at which phase separation occurs were also discovered. Last but not least, it was observed that the thermodynamic model (UNIFAC-LL) properly predicted the behavior of the methanol-water–MTBE ternary system with less than 3% inaccuracy in the binodal curve points. Consequently, a validated phase diagram is developed to accurately predict the physical state of the MTBE-methanol-water system at ant temperature, pressure, and mole fraction of each component. Hence, it guarantees the feasibility of using this tertiary system, as an effective octane booster additive, under severe working conditions.

Quantitative knowledge of competitive adsorption isotherms is essential for the design and optimization of adsorption based separation processes. Since the experimental determination of these thermodynamic functions is complicated and time consuming, there is a need for fast and easy to apply methods. In particular attractive are methods that evaluate measured breakthrough curves (BTC). Key features of these curves can be predicted with the equilibrium theory, which ignores kinetic effects that cause band broadening. If the adsorption equilibria can be described by the classical competitive Langmuir isotherm model, outlet concentration profiles can be calculated analytically. The paper summarizes and illustrates well-known classical results for N -component systems. The theory is applied to analyze experimentally determined BTC for a ternary mixture fed into an initially fully regenerated column under constant flowrate and under isothermal conditions. It is demonstrated that the retention times and intermediate plateau concentrations, which are observable for example in a single ternary BTC experiment, allow estimating a defined number of characteristic equilibrium loadings. These loadings can be directly used for easy estimation of the parameters of an assumed isotherm model. Various possibilities to use a reduced number of loadings and to include complementary results of standard pulse experiments are described. The isotherms generated from the ternary BTC are successfully validated by results of single component and ternary BTC experiments carried out subsequently. Options to generalize the method to determine isotherm model parameters from measured BTC to initially preloaded columns and to more complex mixtures are finally outlined. Highlights An equilibrium theory based dynamic method for determining adsorption isotherms from measured breakthrough curves is described. The method exploits understanding of the column dynamics offered by classical equilibrium theory. It allows estimating characteristic mixture and single component loadings, which can be used to estimate the parameters of an isotherm model. The method is validated analyzing BTC recorded for a ternary system, which follows the competitive Langmuir isotherm model. It is attractive for quickly estimating adsorption capacities and isotherm courses.

Recently, magnetic bio-composites as adsorbent are widely being explored in waste water treatment because of their exceptional properties like high adsorption capacity, selectivity and cost-effective nature. In the present study, a novel recyclable magnetic composite containing magnetic zinc ferrite and alginate in alginic form (ZnFN–Alg) was developed. Various techniques like Fourier Transform-Infra Red, X-ray diffraction, transmission electron microscope with energy dispersive spectra, Brunauer–Emmett–Teller, thermo gravimetric-differential thermal analysis and Point Zero Charge (pH zpc ) were used to characterize the surface morphology of magnetic composite. The magnetic composite was used as adsorbent to remove congo red, crystal violet and brilliant green dyes in single and ternary systems. The kinetic studies data was best fitted to Lagergren pseudo second order whereas mechanism of adsorption was described by intra particle diffusion model in single as well as ternary systems. The adsorption equilibrium data was best fitted to Langmuir isotherm among various adsorption isotherm models. Thermodynamic studies confirmed that the adsorption process was spontaneous in nature. The regeneration ability of ZnFN–Alg composite was studied individually in single and ternary dye systems for seven cycles and showed significant results. It was concluded that magnetic ZnFN–Alg can serve as suitable alternative for the removal of dyes in single and ternary systems.

The double perovskite halides A2BIBIIIX6 provide flexibility for various formulation adjustments and are of less toxicity in comparison with well-discussed complex lead halide derivatives. Such type of structure can be formed by replacing two Pb2+ ions in the cubic lattice with a pair of non-toxic heterovalent (monovalent and trivalent) metal cations, such as silver and indium. The aim of this work is to briefly characterize the phase equilibria in the ternary system CsBr-AgBr-InBr3 and investigate the thermodynamic availability of synthesis of Cs2AgInBr6 double perovskite phase by solid-state sintering or melt crystallization. The results demonstrate the unfeasibility of the Cs2AgInBr6 phase but high stability of the corresponding binary bromides perspective for optoelectronics.

The phase equilibria of the Ag-Al-Au ternary system and the solid-state reaction couple for the Au-xAg/Al system were investigated isothermally at 450 °C. By investigating the Ag-Al-Au ternary system and its isothermal section, this study aims to provide a clearer understanding of the phase stability and interfacial reactions between different phases. This information is crucial for designing materials and processes in electronic packaging, with the potential to reduce costs and improve reliability. There were seven single-phase regions, thirteen two-phase regions, and six three-phase regions, with no ternary intermetallic compound (IMC) formed in the isothermal section of the Ag-Al-Au ternary system. When the Au-25 wt.% Ag/Al couple was aged at 450 °C for 240–1500 h, the AuAl2, Au2Al, and Au4Al phases formed at the interface. When the Ag contents increased to 50 and 75 wt.%, the Ag2Al, AuAl2, and Au4Al phases formed at the interface. When the aging time increased from 240 h to 1500 h, the total IMC thickness in all Au-xAg/Al couples became thicker, but the types of IMCs formed at the interface did not change. The total IMC thickness also increased with the increase in the Ag content. When the Ag content was greater than 25 wt.%, the Au2Al phase was converted into the Ag2Al phase. The IMC growth mechanism in all of the couples followed a reaction-controlled process.

In this paper, the ternary system La2O3-TiO2-Nb2O5 is studied to find new ternary phases with useful electrical properties. The solid solution La3−xTi5−3xNb10−2xO39.5−12.5x was recently identified, and this study focuses on the structural characterization of this solid solution with x = 0.04. The crystal structure, representing a new structural type, was determined from synchrotron and neutron powder diffraction data. The unit cell parameters are a = 7.332 Å, b = 7.421 Å, c = 10.673 Å, α = 84.15°, ß = 80.16°, γ = 60.37°, and space group P1¯. The titanium and niobium atoms are disordered in five different crystallographic sites coordinated octahedrally by oxygen atoms. The eight-coordinated La atoms are embedded in the octahedral framework. Ti and Nb preferentially occupy different sites, and this feature was studied using periodic density functional theory methods. Energies of possible Ti/Nb distributions were calculated and the results agree well with the site occupancies obtained by combined Rietveld refinement of synchrotron and neutron powder diffraction patterns. The geometries optimized by DFT also agree well with the structural parameters determined by diffraction. The general agreement between the theoretical calculations and the experimental data justifies the quantum chemical methods as reliable complementary tools for the structural investigation of ceramic materials.