Soluble Salts Research Articles

Anion‐Anchored Polymer‐in‐Salt Solid Electrolyte for High‐Performance Zinc Batteries

AbstractSolid polymer electrolytes hold promise for addressing key challenges in rechargeable zinc batteries (ZBs) utilizing aqueous electrolytes. However, achieving simultaneous high ionic conductivity, excellent mechanical strength, and a high cation transference number while effectively suppressing Zn dendrites remains challenging. Herein, we design a novel polymer‐in‐salt solid electrolyte (PISSE) composed of polyacrylonitrile (PAN), zinc chloride (ZnCl2), and niobium pentoxide with oxygen vacancies (Nb2O5‐x) with high ionic conductivity. PAN polymer matrix provides the electrolyte good mechanical properties and solubility of Zn salt. The high concentration of ZnCl2 effectively decouples the Zn2+ from polymer chain segments and provides more ionic conduction amorphous region. Moreover, incorporating Nb2O5‐x filler accelerates Zn2+ desolvation by anchoring (ZnxCly)2x–y clusters and enhances the system's mechanical properties, achieving a superior Zn2+ transference number (~0.93) and interfacial stability. Consequently, the optimized PISSE demonstrates exceptional stability during prolonged cycling periods, wide temperature range operation (−40 °C to 60 °C), remarkable flexibility, and compatibility with diverse electrode materials. This study provides valuable insights into the design of solid‐state electrolytes based on ZBs and elucidates their multifunctional prospects.

Dynamics of soluble salts in cooling systems of circulating water supply

A model of the dynamics of soluble salts in the water of cooling systems of circulating water supply was developed based on mass balance principles. The proposed model is expressed in a general form under the assumption of a constant volume of circulating water and non-stationary input and output flows. The model accounts for scenarios where the concentration of soluble salts exceeds their concentration in the circulating water, thereby considering the technological necessity to change the system's power source in the event of an emergency at the feedwater treatment facilities. The developed model enables accurate prediction of the water-chemical regime in both existing and new recirculating cooling systems, sufficient for engineering calculations. It also facilitates the selection of optimal management strategies for such systems, including stabilization methods for recirculating water, feedwater preparation, blowdown volumes, etc. The model was validated under laboratory conditions for cases of concentration and dilution of highly soluble NaCl salt, with an observed error margin not exceeding 2%, attributed to experimental and instrumental factors. The variation in the concentration factor was analyzed for different blowdown rates, assuming initial equality of soluble salt concentrations in feedwater and circulation water. It was shown that establishing dynamic equilibrium between the circulation and feed waters can require dozens or even hundreds of circulation cycles for blowdown rates of 1–4%, and this system inertia must be considered during operation and when forecasting the performance of cooling systems with circulating water supply.

Geochemical evolution of the Dead Sea brine during the last glacial cycle from chemical compositions of interstitial soluble salts

Geochemical evolution of the Dead Sea brine during the last glacial cycle from chemical compositions of interstitial soluble salts

Effect of channel roughness on the particle diffusion and permeability of carbon nanotubes in reverse electrodialysis process applying molecular dynamics simulation

Innovative technology and methods are crucial for making pure and refreshing water. Two main methods are present to delete soluble salts from water: membrane processes and thermal processes. A beneficial membrane technique is reverse electrodialysis. This research used molecular dynamics (MD) simulation to investigate how channel roughness affected particle diffusion and permeability in carbon nanotubes (CNTs) via the reverse electrodialysis process. The results indicate that adding roughness in the CNT duct increased the force between the primary fluid and the duct. Using an armchair-edged CNT structure maximized the electric current in the sample. Furthermore, the roughness increased the intensity of force in the channel, which was due to gravity, leading to a decrease in the mobility of fluid particles. Additionally, several broken hydrogen bonds inside the simulation box increased from 116 to 128 in the duct sample with roughness.

Distribution of Salts in Milk and Cheese: Critical Methodological Aspects

The salt fractions of milk consist of cations (e.g., Ca, Mg, and Na) and anions (e.g., phosphate, citrate, and chloride). These salts are present as free ions or in complexes with other ions or proteins, primarily the caseins. Furthermore, significant levels of Ca and phosphate are also found in insoluble form, inside the casein micelles. The distribution of salts between this micellar phase and the soluble phase is important for the stability and properties of milk and dairy products. Various processes, such as (ultra-)centrifugation, (ultra-)filtration, dialysis, and selective precipitation have been used to separate the micellar and soluble phases in milk and dairy products to allow for studying the salts’ distribution between these phases. These different methods can lead to different levels of soluble salts because the salts in the supernatant from centrifugation, the permeate from ultrafiltration, and the diffusate from dialysis can differ notably. Hence, understanding which components are fractionated with these techniques and how this affects the levels of the soluble salts determined is critical for milk and dairy products. Applying the aforementioned methods to cheese products is further challenging because these methods are primarily developed for fractionating the soluble and micellar phases of milk. Instead, methods that analyze salts in water-soluble extracts, or soluble phases expressed from cheese by pressing or centrifugation are typically used. This review focuses on the significance of salt distribution and variations in salt fractions obtained using different methodologies for both milk and cheese.

Evaluating the impact threshold of soluble salts on preservation of earthen site in Emperor Qin Shi Huang’s mausoleum

The recurrent crystallization and subsequent volumetric expansion of soluble salts pose significant risks to earthen sites, particularly those with archaeological remains on their surfaces. Therefore, timing interventions based on salt content is crucial. This study focuses on the effects of soluble salt content on the earthen site within the burial pits of the Qin Mausoleum, with a particular emphasis on defining safe salinity levels. A mixture of Na2SO4/NaCl salts in a 1:1 mass ratio was added to remodelled soil cakes, which were then aged in a climate chamber for several months. The area of salt expansion on the soil cakes’ surfaces was measured using a deep-focus microscope to assess damage. The results indicate a sudden increase in salt expansion when salinity exceeded 0.1%. Additionally, re-evaluations of these soil cakes years later allowed for the exploration of mechanisms and the feasibility of assessing soil surface expansion and friability at different stages of the earthen site’s lifecycle, including excavation and display. These findings provide preliminary scientific bases and novel methodologies for the further preventive conservation of heritage earthen sites.

Deep eutectic solvent as stationary phase for flow analysis: Automated trace metal determination in food products

BackgroundDeep eutectic solvents (DES) have emerged as effective solvents that address many challenges in analytical chemistry, particularly in microextraction. However, until now, their use has been primarily focused on extraction processes. This has significantly limited their application in analytical chemistry, especially in flow analysis, where the high viscosity of DES has made their use difficult. ResultsThis paper presents a novel DES-based liquid-liquid microextraction approach for the separation and determination of trace metals in foods using an automated flow analysis system. In this study, a DES composed of thymol and thionalide was first prepared and thoroughly characterized by spectroscopic (IR, NMR) and differential scanning calorimetry techniques. The COSMO-SAC model was employed to predict the solubility of metal salts (Cu, Cd, Pb, and Hg) in the new DES. The solvent was applied to glass fiber as a stationary phase in an extraction column in a flow analysis. After microwave digestion of food samples, metals were extracted by this DES in an automated mode and subsequently eluted with an aqueous thiourea solution. The procedure demonstrated limits of detection (LOD) of 6 μg kg−1 for mercury, 4 μg kg−1 for copper, 6 μg kg−1 for lead and 0.6 μg kg−1 for cadmium. SignificanceThis study represents the first application of a DES-based stationary phase in automated flow analysis, significantly enhancing extraction efficiency. The procedure enables precise and reliable determination of trace metals in food products, aligning with green chemistry principles by minimizing waste.

Role of Ionic Strength in Solubility of Salts in India

Purpose: The aim of the study was to assess the role of ionic strength in solubility of salts in India. Methodology: This study adopted a desk methodology. A desk study research design is commonly known as secondary data collection. This is basically collecting data from existing resources preferably because of its low cost advantage as compared to a field research. Our current study looked into already published studies and reports as the data was easily accessed through online journals and libraries. Findings: Ionic strength increases, the electrostatic interactions between oppositely charged ions in the salt and the surrounding ions in the solution are weakened, leading to changes in solubility. Higher ionic strength often results in greater solubility of salts due to the shielding effect, which reduces ion pairing and prevents precipitation. However, in some cases, extremely high ionic strength may lead to the "salting out" effect, where solubility decreases as ions compete for solvation. This relationship is essential in fields like chemistry and environmental science, where understanding solubility is crucial for processes such as crystallization and precipitation reactions. Implications to Theory, Practice and Policy: Debye-hückel theory, van’t hoff factor and colligative properties theory may be used to anchor future studies on the role of ionic strength in solubility of salts in India. Industries involved in chemical manufacturing and wastewater treatment should adopt protocols that account for ionic strength when designing their processes. Policymakers should establish regulatory frameworks that promote the inclusion of ionic strength considerations in environmental assessments.

Irrigation Water Salinity Affects Solute Transport and Its Potential Factors Influencing Salt Distribution in Unsaturated Homogenous Red Soil

As a promising alternative water source to alleviate irrigation water scarcity in red soil regions in southern China, low-quality water could enhance regional water resource utilization and promote sustainable agriculture. However, its soluble salt and ions could affect soil solute distribution and transport, potentially hindering crop growth. Undoubtedly, it is necessary to understand the mechanism of solute transport in red soil under low-quality water irrigation with different water salinity levels. Therefore, a one-dimensional vertical water infiltration experiment and a solute breakthrough experiment were conducted to evaluate the solute transport (soluble salt, Na+, and Cl−) in unsaturated and saturated homogenous red soil at different salinity levels [1 (S1), 2 (S2), 3 (S3), 5 (S5), and 10 (S10) g/L] when irrigated with simulated low-quality water using analytical-grade NaCl. Moreover, the potential factors affecting salt distribution in unsaturated red soil were determined. The findings indicate positive linear relationships between accumulations of three solutes and irrigation water salinity. Generally, the depth of maximum solute concentration increased with the increase in irrigation water salinity. Soluble salt, Na+, and Cl− exhibited early breakthrough and trailing in red soil, but higher irrigation water salinity could reduce PV and retardation. A mobile and immobile water model (MIM) showed that convection was dominant in solute transport in red soil under low-quality water irrigation. D decreased as a power function with increasing irrigation water salinity, while v and R decreased linearly. Furthermore, the red soil can adsorb Cl− resulting from its special charge characteristics under low-quality water irrigation, which may be the main source of salt adsorption. Additionally, v > soil pH > βsalt primarily influenced salt distribution in the 0–40 cm soil profile. This study can provide insights into solute transport in red soil under low-quality water irrigation, facilitating soil fertility and structure, as well as low-quality water irrigation strategy optimization.

Thermodynamic Justification for the Effectiveness of the Oxidation—Soda Conversion of Ilmenite Concentrates

This article presents the results of a thermodynamic analysis of the oxidation soda conversion reactions of minerals in ilmenite concentrates in the temperature range of 373–2273 K. The thermodynamic parameters of pseudorutile, pseudobrukite, and the new minerals, zhikinite and spessartine, were calculated for the first time. It has been established that the most important criterion relating to the stability of titanium minerals and related elements, as well as the reaction properties of the structural oxides of metals and silicon, is their degree of oxidation. Oxides of silicon (IV) and manganese have the best reactivity in solid-phase oxidizing alkaline environments (VI). Modeling this process scientifically substantiates the mechanism involved in the destruction of minerals in ilmenite concentrates in the low-temperature region in the presence of atmospheric oxygen and sodium oxide of soda ash, which are decomposed through the absorption of heat and the evaporation of moisture during the dehydration of hydrated minerals of iron and manganese and the dehydration of the soda–ilmenite batch. Tests conducted during pilot metallurgical production at the Institute of Metallurgy and Enrichment (PMP of JSC) confirmed the feasibility of processing high-chromium and siliceous rutile leucoxene ilmenite concentrates, which are unsuitable for traditional pyro- and hydro-metallurgical enrichment methods, through single-stage oxidation soda roasting, followed by the leaching of easily soluble sodium salts of iron and associated impurities with water and a dilute hydrochloric acid solution. The proposed energy-saving method ensures the production of high-purity (>98%) synthetic rutile while eliminating the formation of strong deposits on the lining of roasting units.

Oxidative Dissolution and the Aggregation of Silver Nanoparticles in Drinking and Natural Waters: The Influence of the Medium on the Process Development.

Currently, there are quite a few data on the ways silver nanoparticles get into the aquatic environment, on their subsequent dissolution in water, and on the release of toxic Ag+ ions. Differences in the experimental conditions hinder the determination of the basic regularities of this process. In this study, the stages of oxidative dissolution of AgNPs were studied, starting from the formation of silver hydrosol in deaerated solution, the reaction of silver with oxygen and with drinking and natural waters, the analysis of intermediate species of the oxidized colloidal particles, and the subsequent particle aggregation and precipitation, by optical spectroscopy, DLS, TEM, STEM, and EDX. In the presence of oxygen, silver nanoparticles undergo oxidative dissolution, which gives Ag+ ions and results in the subsequent aggregation of nanoparticles. The carbonate hydrosol loses stability when mixed with waters of various origin. This is due to the destruction of the electric double layer, which is caused by an increase in the solution's ionic strength and the neutralization of the charge of the metal core. The environmental hazard of the silver nanoparticle hydrosol would noticeably change and/or decrease when the nanoparticles get into natural waters because of their fast precipitation and because the major part of released Ag+ ions form poorly soluble salts with ions present in water.

Different characteristics of the soil in marmot habitats might be one of the factors that influcting Yersinia pestis prevalent in which than pikas.

Marmots are recognized as host animals for plague caused by Yersinia pestis infection. It is unclear that why plague prevalent in marmot rather than other rodents like pikas in the same habitats. This study aims to analyze the differences of the soil characteristics around marmots and pikas burrows to explore the soils factors impacting on different epidemic intensities of Yersinia pestis in these two rodents. Soil samples were collected from within and around marmot and pika burrows, as well as from the nearby areas not inhabited by them and Chinese baseline soil properties as control groups, in the Qilian Mountains of Gansu Province, China. The physicochemical properties and the bacterial 16S rRNA were measured to analyze the characteristics of soils from different groups. Subsequently, the data were analyzed using R studio. The analysis revealed that marmot habitats exhibited distinct soil characteristics, including lower organic matter and alkaline hydrolyzed nitrogen, but higher electrical conductivity and total soluble salts. And soil in marmot areas tended to have higher concentrations of nickel, chromium, and iron, also lower levels of zinc and selenium. Additionally, the alpha diversity of soil microorganisms in marmot habitats was significantly low. Simultaneously, redundancy analysis was conducted, which showed that the low alpha diversity of marmot-soil was influenced by its physicochemical properties. The alpha diversity of the soil was positively correlated with EC, TSS, Na, and Cr, etc., while it was negatively correlated with AHN, OM, Se, Zn, and Fe, etc. These characteristics in marmot habitats, including low levels of organic matter, alkaline hydrolyzed nitrogen, zinc, selenium, and bacterial alpha diversity, as well as high levels of electrical conductivity, total soluble salts, iron, and nickel, played a crucial role in the spread of plague. It was discovered that the unique characteristics of marmot-soils provided essential elements necessary for the survival of Yersinia pestis, including high levels of Fe and Ca, or facilitated the spread of plague. Thus, the transmission of the plague was facilitated.

Biochar, Organic Fertilizer, and Bio-Organic Fertilizer Improve Soil Fertility and Tea Quality

Tea, the world’s second most traded commodity, significantly impacts the economies of producing countries. However, prolonged cultivation leads to soil degradation, particularly through acidification and the depletion of essential nutrients, which adversely affects tea quality. This study investigates the effects of biomass materials—biochar, organic fertilizer, and bio-organic fertilizer—on both tea quality and soil properties. The results revealed that all biomass treatments improved the catechin quality index (CQI) of tea, with bio-organic fertilizer (BOF) yielding the highest CQI at 629.41, followed closely by biochar (624.16) and organic fertilizer (581.34). Soil analysis indicated that biochar increased soil pH from 4.53 to 5.54, total carbon by 194.6% (from 12.61 g kg−1 to 24.42 g kg−1), and nitrogen levels by 11.7% (from 14.91 mg kg−1 to 16.17 mg kg−1), while reducing soluble salts significantly. Furthermore, biomass treatments enhanced enzyme activities, with urease and acid phosphatase increasing by up to 136.6% and 149.5%, respectively. Correlation analysis revealed significant positive relationships, with tea amino acid content correlating with soil total nitrogen (r = 0.62, p < 0.05) and tea polyphenols positively correlating with available potassium (r = 0.60, p < 0.05). This study demonstrates that integrating biomass materials into tea cultivation not only enhances tea quality but also contributes to soil health, supporting sustainable tea garden management practices.

Heavy Metals Distribution in Mangrove Leaves in Various Sudanese Coastal Zones at The Red Sea

<p style="text-align:justify;"><span style="font-family:"Times New Roman",serif;font-size:10.0pt;line-height:107%;">Mangrove ecosystem contamination, especially in the Red Sea region, has caused major concerns on a worldwide scale. The heavy metal accumulation typical of a mangrove species, </span><em><span style="font-family:"Times New Roman",serif;font-size:10.0pt;line-height:107%;">Avicenna marina </span></em><span style="font-family:"Times New Roman",serif;font-size:10.0pt;line-height:107%;">L. (</span><em><span style="font-family:"Times New Roman",serif;font-size:10.0pt;line-height:107%;">A. marina</span></em><span style="font-family:"Times New Roman",serif;font-size:10.0pt;line-height:107%;">) leaves and soluble salts in sediments have not been studied on the Red Sea coast of Sudan.  The present study investigates the two nutrients calcium (Ca) and iron (Fe) and heavy metals such as barium (Ba), titanium (Ti), and strontium (Sr) in the mangrove species </span><em><span style="font-family:"Times New Roman",serif;font-size:10.0pt;line-height:107%;">A. marina</span></em><span style="font-family:"Times New Roman",serif;font-size:10.0pt;line-height:107%;"> in the leaves of six different locations in the Red Sea coastal area, as follows: (Hamasyat (HM) Keligo (KG), and Enkfel (EK) of the Gulf of Dunnabeb, and three sites were selected in the south of the Sudanese coast as follows: (Amarat Island (AM), Ibn Abbas Island (BN), and Ras Kassar (RK). The results demonstrate that the maximum calcium (Ca) and iron (Fe) concentrations in mangrove leaves were 35.9 mg/kg and 4.10 mg/kg recorded at RK and AM, respectively, in the south region of the Red Sea. The heavy metal concentrations (mg/kg) vary between different locations. The higher concentration of heavy metals in mangrove leaves increased as Ba was 1.1 mg/kg in the EG north region. While Ti (0.5 mg/kg) and Sr (2.80 mg/kg) higher concentrations were recorded in AM and EK, respectively, in the south area than in the other experimental sites.   Heavy metals and soluble salts in sediments are continuously monitored in mangrove habitats to ensure they keep within allowed limits. These results could be useful as a database for prospective ecological research, preservation efforts, and long-term sustainable management of the Sudanese mangrove ecosystems throughout the Red Sea coastal.</span></p>

Shattering the Water Window: Comprehensive Mapping of Faradaic Reactions on Bioelectronics Electrodes.

It is generally accepted that for safe use of neural interface electrodes, irreversible faradaic reactions should be avoided in favor of capacitive charge injection. However, in some cases, faradaic reactions can be desirable for controlling specific (electro)physiological outcomes or for biosensing purposes. This study aims to systematically map the basic faradaic reactions occurring at bioelectronic electrode interfaces. We analyze archetypical platinum-iridium (PtIr), the most commonly used electrode material in biomedical implants. By providing a detailed guide to these reactions and the factors that influence them, we offer a valuable resource for researchers seeking to suppress or exploit faradaic reactions in various electrode materials. We employed a combination of electrochemical techniques and direct quantification methods, including amperometric, potentiometric, and spectrophotometric assays, to measure O2, H2, pH, H2O2, Cl2/OCl-, and soluble platinum and iridium ions. We compared phosphate-buffered saline (PBS) with an unbuffered electrolyte and complex cell culture media containing proteins. Our results reveal that the "water window"─the potential range without significant water electrolysis─varies depending on the electrolyte used. In the culture medium that is rich with redox-active species, a window of potentials where no faradaic process occurs essentially does not exist. Under cathodic polarizations, significant pH increases (alkalization) were observed, while anodic water splitting competes with other processes in media, preventing prevalent acidification. We quantified the oxygen reduction reaction and accumulation of H2O2 as a byproduct. PtIr efficiently deoxygenates the electrolyte under low cathodic polarizations, generating local hypoxia. Under anodic polarizations, chloride oxidation competes with oxygen evolution, producing relatively high and cytotoxic concentrations of hypochlorite (OCl-) under certain conditions. These oxidative processes occur alongside PtIr dissolution through the formation of soluble salts. Our findings indicate that the conventional understanding of the water window is an oversimplification. Important faradaic reactions, such as oxygen reduction and chloride oxidation, occur within or near the edges of the water window. Furthermore, the definition of the water window significantly depends on the electrolyte composition, with PBS yielding different results compared with culture media.

Improved in-situ characterization for the scaling-induced wetting in membrane distillation: Unraveling the role of crystalline morphology

Despite being recognized as a promising technique for treating high salinity water, membrane distillation (MD) has been plagued by the scaling of sparingly soluble salts. The growth of crystals can not only create additional resistance to evaporating water at the feed-membrane interface, but also alter the hydrophobic network to bridge the feed and distillate (i.e., result in the phenomenon of wetting). When recognizing the uncertain behaviors of calcium sulfate (CaSO4) scaling in MD, this study was motivated to ascertain whether the crystal-membrane interactions could be dependent on the variation in crystalline morphology. In particular, optical coherence tomography (OCT) was employed to characterize the scaling-induced wetting via a direct-observation-through-the-membrane (DOTM) mode, which mitigated the effects of developing an external scaling layer on resolving the crystal-membrane interactions. The improved in-situ characterization suggests that the crystalline morphology of CaSO4 could be effectively regulated by varying the stoichiometry of crystallizing ions; the richness of calcium in the aqueous environment for crystallization would be in favor of weakening the crystal-membrane interactions. The stoichiometry-dependent growth of CaSO4 crystals can be exploited to develop an effective strategy for preventing the hydrophobic network from being wetted or irreversibly damaged.

Characterization and Classifications of Saline/Sodic Soils of Ambo Area of Irrigated Farm Land in Golina Watershed in Raya Valley, Amhara Region, Ethiopia

All soils are known to contain a certain amount of soluble salts and exchangeable sodium, magnesium, potassium, and calcium. However, excessive enrichment of any one of them can interfere with many soil processes, including plant growth, and the effects depend on the degree of enrichment and the type of plant. Therefore, the objective of this study was to characterize the salt-affected soils of the Ambo area for irrigated farmlands in the Golina Watershed in Raya Kobo Woreda, Amhara region. One profile was excavated from an irrigated field to carry out this activity. One profile was excavated from the irrigated field to conduct this activity. Ten soil samples were taken from the soil profile at 2 m depth at 20 cm depth intervals. The samples were analyzed for several soil physical properties, including soil pH, soluble cations and anions, soluble salts (electrical conductivity, EC), exchangeable cations (Ca, Mg, Na, K), total nitrogen, organic carbon, soluble phosphorus, percent exchangeable sodium, sodium absorption, and soil physical properties (soil color, texture, bulk density, and soil porosity). Chemical properties were also analyzed. The analysis showed that the irrigated farmland soils had a pH of 7.6 to 8.8, electrical conductivity of 1.3 to 14 dsm-1, organic carbon of 0.3 to 1.2%, total nitrogen of 0.11 to 0.35%, soluble phosphorus of 24 to 41.4 mg kg-1, and cation exchange capacity of 50.3 to 65.5 cmol(+) kg-1. The distribution of exchangeable calcium was not consistent across the soil profiles of the irrigated farmlands. In general, the top layer of soil at both sites (because of its agricultural use) was considered for EC, ESP, and pH values. The irrigated farmland soils were classified as saline soils.

INVESTIGATION OF RARE AND RARE-EARTH ELEMENTS LEACHING PROCESSES FROM THE WEATHERING CRUST ORES OF THE KUNDYBAY DEPOSIT

The weathering crust ore of the Kundybay deposit is a hard-enriched ore that contains such minerals as cherchite, bastnesite, kaolinite, etc., which are embedded in the matrix structure of other silicate rocks. These minerals contain rare earth (RE) and rare earth elements (REE). The multi-component structure and dense packing of minerals in the aluminosilicate matrix of the ore make it difficult to be blocking out. Determination of the optimal ore blocking method in order to extract RE and REE is an urgent task for today. The purpose of this work is to develop an effective method of leaching RE, REE and "white soot" from the weathering crust ores of the Kundybay deposit. Methods. Processing with soluble ammonium, magnesium and aluminium salts will allow estimation of the state of RE and REE in the ore. The indicator of RE and REE blocking out during leaching with sodium hydroxide is the transfer of silica into solution, due to which RE and REE form their own hydroxides, which can be subsequently transferred into solution by acid treatment. Acid leaching with sodium pyrosulfite, hydrofluoric acid and sulfuric acid will allow the RE and REE to be immediately transferred into solution. Results and Discussion. The main characteristics of the Kundybay deposit weathering crust ore were determined, such as: silica content, moisture content, base metals, RE and REE. Conclusion. The degree of extraction of RE and REE by soluble salts of ammonium, magnesium and aluminium did not exceed 2%, which indicates the existence of RE and REE in the form of their own minerals. Leaching with sodium hydroxide showed low recovery of silica, with RE and REE remaining in a difficult-torecover form. Leaching with a mixture of sodium pyrosulfite, hydrofluoric and sulfuric acids is a promising method for RE and REE recovery due to the complex effect of the components of this mixture.

EXTRACTION AND CONCENTRATION OF RHENIUM FROM NITRATE-CONTAINING RHENIUM DESORBATE

Extraction technology plays a key role in the industrial production of rhenium, accounting for more than 70% of the world's production of this element. In aqueous and alkaline solutions, rhenium is present in the form of the anion ReO4 - , which necessitates the use of anion exchange extractants based on tertiary amines. Despite the widespread application and many years of research on rhenium extraction with amines, the obtained data remain contradictory. The extraction of rhenium from aqueous solutions by an amine extractant occurs through an anion exchange mechanism with the formation of the complex TAAHReO4. To increase the solubility of amine salts in the organic phase, high-molecular-weight aliphatic alcohols, such as decyl alcohol, are added, which act as modifiers of the organic phase without extracting rhenium themselves. The aim of this work is to investigate the extraction of rhenium with trialkylamine from a model solution that simulates the composition of nitrate desorbate obtained from the processing of uranium ores. Specifically, various factors affecting the extraction and reextraction of rhenium are studied to determine the optimal parameters of these processes. The study uses trialkylamine as the extractant and decyl alcohol as the modifying additive. The results of the study show that the optimal parameters for rhenium extraction are: an extractant concentration of TAA:DA:kerosene=40:5:55 (% by volume), an organic to aqueous phase ratio of V_org/aq = 1:5, an extraction time of 5 minutes, and a rhenium extraction rate of up to 75%. Similar results were obtained with an extractant concentration of TAA:DA:kerosene = 30:10:60 and an extraction time of 5 minutes, where the rhenium extraction rate was about 74%. The re-extraction of rhenium is most efficiently carried out using an ammonia solution with a concentration of 114 g/L NH3⋅H2O and a phase contact time of 10 minutes, with a re-extraction rate of 85.5%. Similar results were obtained with the addition of 174 g/L (NH4)2SO4, where the rhenium re-extraction rate was 82%.

Effect of In Situ Polymerization of Super Absorbent Polymers on the Protection of Earthen Heritage Sites in Semi-Arid Regions

As precious cultural heritage, earthen sites are susceptible to various natural factors, leading to diverse forms of degradation. To protect earthen sites, the effects of super absorbent polymers (SAPs) on soil water retention, physical properties, and color compatibility at different concentrations were studied. After applying SAP treatment to an earthen site with different degrees of weathering, we drew the following conclusions. SAP-2 improved soil water retention capacity, increased soil water content, and slowed down the precipitation of soluble salts. At the same time, SAP-2 had the least effect on soil color difference and reduced the development of cracks by filling soil pores and enhancing the cohesion between soil particles, thus giving the earthen sites better weathering resistance. Therefore, the results provide a useful reference for the surface cracking of earthen sites in semi-arid areas and the degradation caused by flaking and block spalling.