Crystallization Of Blends Research Articles

Tailoring electronic structure and thermodynamic stability of (Al, In)-substituted GaAs: Ab-initio insights into bulk and (001) surfaces

Ab-initio calculations are conducted to investigate the structural properties, electronic structure, and thermodynamic stabilities of bulk and (001) surface systems of the GaAs semiconductor in its zinc-blende crystal phase. For the bulk case, we focus on the impact of substituting gallium atoms with M atoms (M = Al, In) at various concentrations (5.55 %, 11 %, and 22 %). We present the resulting structural parameters, along with the formation and substitutional energies associated with these substitutions. For surface systems, we explore indium (In) or aluminum (Al) substitutions at coverages of 0.25, 0.50, and 1.0 monolayers. This includes investigating the effects of substituting M atoms within the first atomic layer of the slabs. Ab-initio thermodynamic calculations reveal that high Al substitutions, in both bulk and surface, result in more favorable formation and surface energies. In contrast, In substitutions exhibit the opposite behavior, with increasing In content leading to less favorable energetics. Moreover, density of states analysis reveals that bulk systems maintained a semiconducting character, while all studied surface configurations exhibited a metallic electronic behavior. This study provides valuable insights into the influence of Al and In substitutions on the structural, electronic, and thermodynamic properties of GaAs, both in bulk and on the (001) surface.

Estimating the activation energy of crystallization in blends of poly L‐lactic acid and poly(propylene 2,5‐furan dicarboxylate) during isothermal melt crystallization using temperature dependent infrared spectroscopy

Estimating the activation energy of crystallization in blends of poly L‐lactic acid and poly(propylene 2,5‐furan dicarboxylate) during isothermal melt crystallization using temperature dependent infrared spectroscopy

High-quality thickness-tunable InAs nanowire crosses grown by molecular-beam epitaxy

InAs nanowire crosses show great potential applications in detection and braiding of Majorana zero modes. Controlled growth of high-quality and diameter tunable InAs nanowire crosses is fundamental for these applications. However, it is still difficult to freely and conveniently adjust the diameter of the free-standing InAs nanowire crosses grown by the conventional growth methods. Here, we report a new technique to realize the growth of high-quality thickness-tunable InAs nanowire crosses by molecular-beam epitaxy. GaAs nanowire crosses were firstly grown on the Si (100) substrates spontaneously by merging the <111>-oriented GaAs nanowires. InAs nanowire crosses were then obtained by in situ growth of InAs shells on the facets of GaAs nanowire cross cores. Detailed scanning and transmission electron microscopic observations and energy dispersive spectrum analyses confirm that the InAs nanowire crosses grown by this manner have continuous and smooth morphology and they are high-quality zinc-blende crystals. More importantly, the InAs shell is grown with the vapor-solid growth mechanism and the thickness of the InAs nanowire crosses can be tuned by varying the InAs shell growth time. Our work provides a valuable method for the controlled growth of thickness-tunable semiconductor nanowire crosses.

Determination of the discreteness correction in dislocation equations for sphalerite crystals

Abstract The discreteness correction for simple lattices has been determined, however, there is still no detailed and rigorous derivation of the discreteness correction for compound lattices due to the relatively complex structure (simple lattices have only one set per slip system, while complex lattices have at least two sets). A lattice dynamics model which takes into account the energy increments caused by changes in bond length and bond angle is constructed for sphalerite crystals and the relationships between discreteness parameters and elastic constants are determined for the slip system. Compared to glide set, the discreteness correction for shuffle set is much larger due to it is mainly contributed by the interactions between nearest neighbor atoms. Based on the results obtained from the model, the dislocations in ZnS crystal are investigated. The theoretical prediction result of Peierls stress for shuffle dislocation closely matches the experimental critical shear stress. It is inferred that the initial plastic deformation of ZnS is closely related to the movement of shuffle dislocations.

Low field mobility in bulk GaN and its ternary AlGaN/GaN compounds (quantum kinetic approach)

Analytical expressions for the low-field mobility of charge carrier gases with three-(3D), two-(2D) and one-(1D) dimensionalities are obtained. Multi-ion ionized impurities scattering, acoustic and polar optic phonons are considered as scattering mechanisms. The calculated values of mobility are compared to known experimental data for bulk (3D) n-and p-type wurtzite, n-type zinc-blende GaN crystals and low dimensional (2D and 1D) ternary GaAlN compounds. The resulting analytical expressions give the dependences of mobility on dimensionality of charge carrier gas, its density, effective mass, temperature and confining dimensions. A comparison of the experimental and calculated temperature dependences of the mobility in bulk GaN crystals (3D) and in AlGaN/GaN nanowires (1D) shows that the mobility at 100\\,{\ ext{K}}$?> T>100K is determined by the scattering of charge carriers by polar optical phonons with an energy of 91.2 meV. The temperature dependences of mobility in Al0.25Ga0.75N/GaN heterostructures (2D) at 100\\,{\ ext{K}}$?> T>100K are in consistent with experiment for electron scattering by polar optical phonons with a noticeably higher energy of 160 meV. We associate this fact with the heterointerface, which according to well-known theoretical studies can change both the strength of electron polar optical phonons scattering and the energy of the phonons.

Influence of volume expansion in NaCl crystallization on the physical properties and molecular structure of asphalt: A MD simulation study

The pavement damage caused by salt-induced volume expansion is becoming increasingly noticeable. Molecular dynamics (MD) method was applied to evaluate the effects of varied volumes of NaCl crystals on physical properties and structure of asphalt. The effects of NaCl crystals on the compatibility between styrene–butadiene–styrene triblock copolymer (SBS) and asphalt, as well as the influence of SBS on the diffusion coefficient of NaCl crystals in the asphalt system, were investigated alongside their effects on the physical modulus and molecular structure of asphalt. The results show that the solubility parameter of the asphalt blends decreases as the volume of NaCl crystals increases. Specifically, the solubility parameter decreases by 52.5 % for the biaxial crystalline growth of NaCl and asphalt blends compared to the matrix asphalt. The analysis of the ion diffusion coefficient reveals that the primary disruption of NaCl crystals in asphalt blends is due to early Cl- and late Na+ diffusion. Furthermore, the rise in shear modulus of the asphalt blends suggests that the salt erosion process of SBS-modified asphalt is advantageous for its high temperature and shear resistance. The changes in peak radial distribution function and radius of gyration indicate that the inclusion of NaCl and SBS into asphalt is a physical aging process. In this case, SBS incorporation acts as a reinforcement to the asphalt to retard the erosion of NaCl.

Electronic and Optical Properties of Mn-Doped HgSe Topological Insulator for Spintronic Devices

HgSe is a Mercury chalcogenide material of the HgX family (where X = S, Se, Te) which crystallises in the zincblende crystal phase. The electronic band structure of HgSe is indicative of a new state of matter in the condensed phase that is of great interest for fundamental physics and possibly new applications. This paper reports ab-initio calculations of the structural, electronic, magnetic, and optical properties of zincblende Mercury selenide (HgSe) doped with manganese (Mn) in the inter sites HgMnxSe, with x = 0, 0.058, and 0.117, using the framework of spin-polarized density functional theory (SP-DFT). The aim of our investigation is to discuss the different properties of this doped material in order to improve the promising new domain of spintronics with topological systems. Both the GGA + U + mBJ approach and spin–orbit coupling (SOC) are used for band structure calculations and density of states. The results show a nontrivial topological semimetal order for HgSe and a ferromagnetic topological and metallic behaviour for HgMnxSe. The frequency response of optical properties shows interesting characteristics. Furthermore, the variation with concentration x of the critical point for each of the optical parameters is similar to that of the inverted band gap.

Selective area growth of in-plane InAs nanowires and nanowire networks on Si substrates by molecular-beam epitaxy

In-plane InAs nanowires and nanowire networks show great potential to be used as building blocks for electronic, optoelectronic and topological quantum devices, and all these applications are keen to grow the InAs materials directly on Si substrates since it may enable nanowire electronic and quantum devices with seamless integration with Si platform. However, almost all the in-plane InAs nanowires and nanowire networks have been realized on substrates of III–V semiconductors. Here, we demonstrate the selective area epitaxial growth of in-plane InAs nanowires and nanowire networks on Si substrates. We find that the selectivity of InAs growth on Si substrates is mainly dependent on the growth temperature, while the morphology of InAs nanowires is closely related to the V/III flux ratio. We examine the cross-sectional shapes and facets of the InAs nanowires grown along the 〈110〉, 〈100〉 and 〈112〉 orientations. Thanks to the non-polar characteristics of Si substrates, the InAs nanowires and nanowire networks exhibit superior symmetry compared to that grown on III–V substrates. The InAs nanowires and nanowire networks are zinc-blende (ZB) crystals, but there are many defects in the nanowires, such as stacking faults, twins and grain boundaries. The crystal quality of InAs nanowires and nanowire networks can be improved by increasing the growth temperature within the growth temperature window. Our work demonstrates the feasibility of selective area epitaxial growth of in-plane InAs nanowires and nanowire networks on Si substrates.

Material characteristics governing in-plane phonon-polariton thermal conductance

The material dependence of phonon-polariton-based in-plane thermal conductance is investigated by examining systems composed of air and several wurtzite and zinc-blende crystals. Phonon-polariton-based thermal conductance varies by over an order of magnitude (∼0.5–60 nW/K), which is similar to the variation observed in the materials corresponding to bulk thermal conductivity. Regardless of the material, phonon-polaritons exhibit similar thermal conductance to that of phonons when layers become ultrathin (∼10 nm), suggesting the generality of the effect at these length-scales. A figure of merit is proposed to explain the large variation of in-plane polariton thermal conductance that is composed entirely of easily predicted and measured optical phonon energies and lifetimes. Using this figure of merit, in-plane phonon-polariton thermal conductance enlarges with increases in (1) optical phonon energies, (2) splitting between transverse and longitudinal mode pairs, and (3) phonon lifetimes.

Crystallinity and Oscillatory Shear Rheology of Polyethylene Blends.

Crystallinity and rheological behavior are significant for processing semi-crystalline polymers with fine mechanical properties. There is always an economical need to create a less expensive new material with better properties. Non-isothermal crystallization and oscillatory shear rheology of different branch-type polyethylene-polyethylene blends were investigated. Samples of high-density and low-density polyethylene (HDPE/LDPE) (20/80, 40/60, 60/40 and 80/20 weight ratios) and two types of high-density and linear low-density polyethylene (HDPE/LLDPE) (40/60 and 60/40 weight ratios) were prepared via extrusion. The materials were tested by differential scanning calorimetry (DSC) at several cooling rates (5, 10, 20, 30 and 40°/min) and by oscillation rheometry (ARES G2) at low angular frequency range to prove their miscibility or immiscibility. It was found that the one-peak melting endotherm of the 80-20% HDPE-LDPE blend could indicate miscibility in the solid phase, while the other HDPE-LDPE blends with two-peak curves are partially or not miscible. In contrast, all the HDPE-LLDPE blends indicate co-crystallization, but the 40-60% HDPE-LLDPE butylene blend is probably immiscible. It was revealed that complex viscosity decreases with angular frequency: linearly for HD-LD blends and not linearly for HD-LLDPE blends. The complex viscosity shows linear behavior with composition for HD-LLDPE blends, while there is a positive-negative deviation for HD-LD blends. In the liquid phase, according to rheological measurements, the HDPE-LDPE blends are not or partially miscible, while the HDPE-LLDPE blends are probably miscible.

Defining the physical properties of blends of acetyl‐triacylglycerols derived from transgenic oil seeds

AbstractAcetyl‐TAG are unusually structured triacylglycerols (TAG) that possess an acetate group at their sn‐3 position. Acetyl‐TAG have different physical properties compared to regular TAG, including lower viscosity and improved cold temperature properties, making acetyl‐TAG useful for different applications, including as a diesel replacement. These unusual TAG molecules can be synthesized in the seeds of transgenic plants through the expression of diacylglycerol acetyltransferase (DAcT) enzymes isolated from different Euonymus species. In this study, the kinematic viscosity as well as the crystallization and melting behavior of blends of acetyl‐TAG and regular TAG were examined to define goals for acetyl‐TAG synthesis in transgenic plants. Even small amounts of regular TAG when blended with acetyl‐TAG had a disproportionate effect on the viscosity of mixture. This effect of regular TAG in increasing kinematic viscosity was more pronounced at lower temperatures. Under slow cooling conditions, the two different TAGs and their blends possessed two main crystallization events with different degree of separation of the thermal transition, and the lower crystallization temperature decreased with increasing amounts of acetyl‐TAG in the blend. At higher cooling rates, one broad and tailed crystallization peak was observed. Heating thermograms indicate similar polymorphic behavior of the blends and a general peak shift to lower transition range with increasing acetyl‐TAG compared to the two pure lipids. This information about the viscosity and thermal properties of blends of TAG and acetyl‐TAG will provide useful targets for engineering higher levels of acetyl‐TAG in transgenic seeds.

Using ML8 to achieve the lime-free separation of sphalerite-pyrrhotite under the copper activation system

Sphalerite flotation is conducted under Cu2+ activation system, whereas the selective separation of pyrrhotite is difficult due to the inevitable activation effect of Cu2+, which requires a large amount of lime to depress pyrrhotite flotation. In this study, the conventional collector butyl xanthate and a novel collector ML8 were compared to the selectivity of the flotation separation of sphalerite and pyrrhotite. The ML8 was investigated as an effective sphalerite collector to achieve the lime-free separation of sphalerite and pyrrhotite. Single mineral flotation indicated that sphalerite exhibited good floatability under low-alkaline conditions, whereas pyrrhotite was almost non-floatable, and their selective separation could be achieved using a low dosage of ML8. Mixed mineral flotation further confirmed that the ZnS separation could be achieved under low-alkaline conditions (pH = 9) using ML8 as a sphalerite collector. Reagents adsorption measurements demonstrated that ML8 possessed greater affinity to sphalerite than pyrrhotite, thus the contact angle of sphalerite increased from 51° to 76° after treatment with ML8 while that of pyrrhotite only increased from 67° to 70°. XPS detection results illustrated that the adsorption sites of ML8 on sphalerite were the adsorbed Cu site on the mineral surface rather than the Zn site of sphalerite crystal. The amount of Cu sites located on sphalerite was much greater than on pyrrhotite after the activation with copper sulfate.

Effects of molecular weight on stereocomplex and crystallization of PLLA/PDLA blends

The chain dynamics affects the chain motions and the crystallization behaviors of polymers, and the crystallization ability of poly(lactic acid) (PLA) homopolymers can be substantially enhanced by incorporating stereocomplex-PLA (s-PLA). The effects of s-PLA molecular weight on the enhanced crystallization of the homopolymer were characterized and analyzed in this study. The crystallization behaviors, morphologies and structures of the homopolymer in PLA/s-PLA blends were investigated using DSC, POM, WAXD and FTIR during or after isothermal and non-isothermal crystallization. The blends compose homopolymer and the same content of the s-PLAs with three different molecular weights. The DSC results showed that the homopolymer in the blends containing the higher molecular weight of the s-PLA crystallizes at higher crystallization temperature than that containing the lower molecular weight of the s-PLA during the non-isothermal crystallization. The crystallization half-time of the homopolymer blending with the higher molecular weight s-PLA is shorter than that blending with the lower molecular weight of the s-PLA during the isothermal crystallization. POM images showed that the spherulite density of the homopolymer blending with the higher molecular weight of the s-PLA is significantly higher than that with the lower molecular weight of the s-PLA. The Mpemba effect was first experimentally observed in the melting crystallization of polymer blends containing PDLA and s-PLA. A possible explanation is proposed and discussed to elucidate the impact of s-PLA molecular weight on the crystallization behaviors of PLA homopolymer in the blends.

The origin and ore-forming processes of the Qixiashan Pb–Zn–Ag deposit, South China: Constraints from LA–ICP–MS analysis of pyrite and sphalerite

The Qixiashan Pb–Zn–Ag deposit, located in the Nanjing–Zhenjiang area of the Middle–Lower Yangtze Metallogenic Belt (MLYB), is one of the largest PbZn deposits in Eastern China. The middle Carboniferous carbonates of the Huanglong Formation are the main host rocks of orebodies. Whether this deposit is associated with magmatic activity or sedimentary exhalative deposit is still debated due to the poor constraints on the origin of the ore materials and metallogenic processes. To address this, we analyzed the compositions of pyrite and sphalerite from different mineralization stages and depths, and the distributions of minor and trace elements within the pyrite and sphalerite crystals, using in situ laser ablation–inductively coupled plasma–mass spectrometer and scanning electron microscope analyses. Four hydrothermal stages can be identified: the pre-ore pyrite stage (stage I); Pb–Zn–Py stage (stage II); Pb–Zn–Ag stage (stage III); and carbonate stage (stage IV). The sphalerite in the deposit is typically enriched in Fe, Mn, In, and Sn, and depleted in Ge and Cd. These results are characteristic of magmatic hydrothermal activity and indicate the mineralization was related to late Yanshanian magmatic activity. The Co and Ni contents of pyrite, and the Fe, In, and Sn contents of sphalerite decrease from the early to late stages, suggesting that the temperature of the hydrothermal fluid decreased continuously. Variations in the Se content of pyrite suggest that the fO2 increased from stage I to stage II, then decreased during stage III. Detailed SEM and elemental maps show that stage-II sphalerite (Sph-1) and pyrite (Py-2) are oscillatory zoned, which we interpret to reflect pressure fluctuations and repeated local fluid phase separation during stage II. We also infer from the zoning and subsequent formation of Py-3 that magmatic hydrothermal activity increased from stage I to II, then decreased from stage II to III. In addition, changes in the In, Sn, and Fe contents of sphalerite can be useful indicators of the upward migration of ore-forming fluid and can help during prospecting for related deep magmatic rocks.

Direct generation of a terahertz vector beam from a ZnTe crystal excited by a focused circular polarized pulse.

A vector beam is a type of topological beam in which the polarization direction of light rotates around a singularity on the wavefront. This paper proposes a method to generate a vector beam by tightly focusing a pump beam in the crystalline direction such that the second-order nonlinear optical effect is forbidden. The directional dependence of the effective nonlinearity in zincblende crystals, such as ZnTe, was analytically investigated. Two types of nonlinear polarization singularities were found in [111] and [100] directions. Their polarization topological charge ℓ was +1 and -1, respectively. To experimentally demonstrate the proposed method, a (111) cut ZnTe crystal was selected as the nonlinear crystal. The polarization state of the generated terahertz (THz) beams was measured with a custom-built THz spectroscopic polarization imaging system. Radially polarized distributions were observed within the entire generated spectral region. Such a broadband feature of the generated vector beam is likely due to the topological nature of the focused pump beam, where the wavevectors are winding once about the optical axis. This simple method for generating THz vector beams will accelerate its applications.

Exceptional X-Ray contrast: Radiography imaging of a Middle Triassic mixosaurid from Svalbard.

The black shales of the Middle Triassic Botneheia Formation in Svalbard are known for their fossil richness with abundant ichthyosaur remains and beds of the bivalve Daonella. Vertebrate remains from the Muen Mountain on Edgeøya are shown to have exceptional X-ray contrast due to a combination of sulphide and sulphate permineralisation and pseudomorphing. Radiography imaging of a previously described specimen, PMO 219.250, revealed new and spectacular details such as more carpals, teeth, and skull sutures. Teeth and skull characters are taxonomically significant. supporting the referral of PMO 219.250 to Phalarodon and further suggesting an affinity to P. atavus. Three sulphur phases were identified, with the sulphide sphalerite (ZnS) being the highest temperature phase, followed by the sulphate baryte (BaSO4), and the sulphide pyrite (FeS2). Sulphate permineralisation is also seen in specimens from the Upper Jurassic on Svalbard. We suggest that sulphur-rich fluids have flowed and dissolved barium from the shales and deposited the sphalerite and baryte, and that this could be linked to the Cretaceous HALIP. The Jurassic specimens are only permineralised by baryte, while the Triassic specimens have also been permineralised, but mainly pseudomorphed by baryte with crystals of sphalerite. Lithology differences appear to have controlled the compaction of the Triassic specimens, while the Jurassic specimens have retained their three-dimensional shape due to the baryte emplacement relatively earlier in their depositional history. Although soft tissues are not preserved, the excellent X-ray contrast in the Middle Triassic specimens is reminiscent of pyritised fossil sites such as the Hunsrück Slate (Devonian), Beecher's Trilobite Bed (Ordovician), and the La Voulte-sur-Rhône marls (Jurassic).

Electrolytes for Zn Batteries: Deep Eutectic Solvents in Polymer Gels.

Gel polymer electrolytes composed of deep eutectic solvent acetamide4 :Zn(TFSI)2 and poly(ethylene oxide) (PEO) are prepared by using a fast, solvent-free procedure. The effect of the PEO molecular weight and its concentration on the physicochemical and electrochemical properties of the electrolytes are studied. Gels prepared with ultrahigh molecular-weight PEO present pseudo-solid behavior and ionic conductivity even higher than that of the original liquid electrolyte. A decrease in the dendritic growth in soft gels with PEO contents up to 1 wt % is demonstrated. The changes in the chemical structure of the electrolyte produced by the strong interactions between ethylene oxide units and Zn2+ have also been studied. The addition of PEO takes the electrolyte out of its original eutectic composition, producing blend crystallization. However, it is possible to retain the eutectic point of the electrolyte in a gel form if the addition of PEO is accompanied by the reduction of acetamide.

Generation of nonlinear polarization to emit terahertz waves in above gap states in GaSb/AlGaSb multiple quantum wells

In this study, we report the generation of frequency-tunable even-order nonlinear polarization in the above gap states in strained multiple quantum wells. Using the strain field, the even-order polarization to emit terahertz waves is generated in a zincblende crystal. Our results can make the material and laser choice ranges wide because the exciton resonant excitation is unnecessary.

Blending of the Thermodynamically Incompatible Polyvinyl Chloride and High-Pressure Polyethylene Polymers Using a Supercritical Fluid Anti-Solvent Method (SEDS) Dispersion Process.

The experimental solubility data of polyvinyl chloride (PVC) and high-pressure polyethylene (HPPE) in organic solvents (toluene, dichloromethane, and chloroform) at temperatures ranging from 308.15 to 373.15 K at atmospheric pressure are reported in the present paper. The solubility of the polymers (PVC and HPPE) in organic solvents (toluene, dichloromethane, and chloroform) was studied at temperatures between 298 and 373 K. The supercritical SEDS dispersion of PVC and HPPE polymer blends at pressures between 8.0 and 25 MPa and at temperatures from 313 to 333 K are reported in the present work. The kinetics of crystallization and phase transformation in polymer blends obtained by blending in a melt, and using the supercritical SEDS method, have been studied. The effect of the HPPE/PVC ratio on the thermal and mechanical characteristics of the polymer blends has been studied. For all studied polymer blends and pure polymers obtained using the SEDS method, the heat of fusion ΔfusH exceeds the values obtained by blending in the melt by 1.5 to 5) times. The heat of fusion of the obtained polymer blends is higher than the additive value; therefore, the degree of crystallinity is higher, and this effect persists after heat treatment. The relative elongation decreases for all polymer blends, but their tensile strength increases significantly.

Thermometric and chemical studies of fluid inclusions in sphalerite from Rhodope lead-zinc deposits: Shumachevski Dol – Gyudyurska (Madan District) and Kenan Dere (Laki District), Bulgaria

The objects of this study are fluid inclusions in sphalerite crystals or selected parts of them from two Central Rhodopean deposits: Shumachevski Dol – Gyudyurska (Madan District) and Kenan Dere (Laki District). A set of data for temperature of homogenization and total salinity are presented. The locations of coupled data in coordinates Th vs total salinity reveal that the Kenan Dere sphalerite has been deposited from solutions of higher temperature (280–374 °C) and lower salinity (2–5 wt.% NaCl-eqv.). Conversely, the Shumachevski Dol and Gyudyurska sphalerites show lower Th = 200–230 °C and somewhat higher salinity (S = 6–12 wt.% NaCl-eqv.). Furthermore, it is likely that both late Kenan Dere and Gyudyurska sphalerites were deposited at 30–50 °C lower temperatures than the earlier ones. Additionally, Decrepitation Inductively-Coupled-Plasma Atomic-Emission-Spectrometry was applied to determine the cations in the inclusion solute. The vacuum decrepitation was also used for liberating the volatiles (H2O, CO2) and analysing them by mass spectrometry. On that account, more detailed preliminary studies of the process of decrepitation were performed. However, the Zn-concentration in sphalerite-hosted fluid inclusions cannot be evaluated and the results from syngenetic quartz offer the only possibility for obtaining information about ore-element content. On the basis of a compilation of both present and previously published data, it can be concluded that the hydrothermal fluid under the Central Rhodope Dome was constituted in situ as a closed system at a depth of ~1 km, under nearly lithostatic pressure (~200 bars), T ≥ 350 °C, and NaCl-dominated salt content ~10%. Under these conditions, a solution with a pH of ~4.0–4.5 contains ore elements (Fe, Zn, Pb) as soluble chlorido-complexes; for Zn, the total concentration may reach 1 wt.%. Sulphide-S compound under these conditions is H2S. The sphalerite deposition follows a reverse path of the chemical reactions. The elevation of the hydrothermal fluid along the extensional dislocations results in boiling (i.e., separation of CO2) and cooling. The temperature decrease destabilizes the chlorido-complexes and leads to an increase in the Zn2+ activity. On the other hand, CO2 loss enhances pH, and thus dissociates H2S, yielding HS- and S2- ions, needed for sphalerite deposition.