Inorganic Salt Solutions Research Articles

Nanoarchitectonics of SiO2 composite hydrogel in inorganic solution: Simulation and experimental analysis

Polyacrylamide hydrogels are widely used in medicine, petrochemical, water treatment and other fields, among which polyacrylamide hydrogels play an important role in oilfield Profile control and water shutoff and enhanced oil recovery, however, there are few reports on the effect of different inorganic salt solutions on the properties of SiO2 composite hydrogel. In this paper, a cross-linked SiO2 composite hydrogel was constructed using Materials Studio software for the first time, and its structure and properties in inorganic salt aqueous solutions were studied. The results show that the addition of inorganic salts can weaken the interaction between water molecules and hydrogels, and this effect is minimal in calcium chloride solution. The radial distribution function shows that there are strong hydrogen bonds between nitrogen and oxygen atoms in the amide group and water molecules, but there are van der Waals forces between oxygen and water atoms, and the addition of inorganic salts will enhance the hydration of nitrogen atoms in the amide group and the interaction between monovalent ions and amide groups was greater than that between bivalent ions. At the same time, the addition of inorganic salts can also enhance the diffusion ability of water molecules and the fluidity of polymer chains. Among the four inorganic salt solutions, Calcium chloride solution has the least effect on the polymer chain and the cross-linked SiO2 composite hydrogel has the best expansion performance in calcium chloride solution, which is basically consistent with the experimental results, this has a potential application prospect in the reservoir with high calcium content for profile control and water plugging and enhanced oil recovery.

Experimental and Modeling Study on Methane Hydrate Equilibrium Conditions in the Presence of Inorganic Salts.

The aim of this study was to determine the influence of four inorganic salts, KCl, NaCl, KBr and NaBr, on the thermodynamic conditions of methane hydrate formation. In order to achieve this, the vapor-liquid water-hydrate (VLWH) equilibrium conditions of methane (CH4) hydrate were measured in the temperature range of 274.15 K-282.15 K by the isothermal pressure search method. The results demonstrated that, in comparison with deionized water, the four inorganic salts exhibited a significant thermodynamic inhibition on CH4 hydrate. Furthermore, the inhibitory effect of Na+ on methane hydrate is more pronounced than that of K+, where there is no discernible difference between Cl- and Br-. The dissociation enthalpy (∆Hdiss) of CH4 hydrate in the four inorganic salt solutions is comparable to that of deionized water, indicating that the inorganic salt does not participate in the formation of hydrate crystals. The Chen-Guo hydrate model and N-NRTL-NRF activity model were employed to forecast the equilibrium conditions of CH4 hydrate in electrolyte solution. The absolute relative deviation (AARD) between the predicted and experimental values were 1.24%, 1.08%, 1.18% and 1.21%, respectively. The model demonstrated satisfactory universality and accuracy. This study presents a novel approach to elucidating the mechanism and model prediction of inorganic salt inhibition of hydrate.

Recurrently gellable and thermochromic inorganic hydrogel thermogalvanic cells.

Thermogalvanic cells (TGCs) draw great attention in the field of heat to electricity conversion, but TGCs were only in the form of liquid or organic gel. Here, we report an all-inorganic hydrogel TGC via simply mixing and stirring two inorganic salt solutions. Benefiting from the hydrogen bonds resultant framework and endogenous Fe2+/3+ redox couple, the TGC can recurrently pulverize-gel with completely holding its initial thermogalvanic performances after even 60 cycles. As the temperature and pH coregulating Fe3+ concentration and reversible transformation between Fe3+ and Fe(OH)3, we boost thermopower and realize thermochromism. This work provides a different perspective for TGCs and offers an avenue for future hydrogel materials research.

Polyvinylidene fluoride-based loose nanofiltration membrane with graphene oxide intercalation for efficient small organic molecules desalination

Graphene oxide (GO) loose nanofiltration (LNF) membranes show immense potential for the desalination of small organic molecules. However, it remains a significant challenge to compare the performance of GO LNF membranes prepared via different doping methods and study the mechanisms that influence the separation abilities of the membranes. In this study, LNF membranes prepared via three GO doping methods were examined for flux, retention rate, and the separation performance of small organic molecules and inorganic salts. The membranes coated with dopamine (DA) and GO, and subsequently formed polydopamine (PDA)–GO intercalation, showed the best results. A novel LNF membrane material (PVDF/PDA–GO–TFN; PVDF: polyvinylidene fluoride, TFN: thin-film nanocomposite) was developed to enhance the separation performance of small organic molecules and inorganic salts while improving membrane surface stabilization and anti-fouling performance and reducing the “trade-off” effect. The optimal conditions for PDA–GO intercalation and the best combination for interfacial polymerization (IP) were also determined. The intercalation structure was identified via scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy, atomic force microscopy, and Fourier-transform infrared spectroscopy. Furthermore, the separation mechanism of the membrane was determined to be based on the Donnan and steric hindrance effects, according to the correlation analysis of the membrane surface electrical properties (zeta potential), hydrophilicity (contact angle), and pore properties. The PVDF/PDA–GO–TFN LNF membrane displayed a maximum water permeance of 10.45 L/(m2·h·bar), with an 88 % rejection of PEG2000 and a 6.83 % rejection of Na2SO4. Moreover, the membrane exhibited excellent anti-fouling performance and long-term stability, with a mean flux recovery rate of 99.06 % after four cycles of filtration and backwashing tests using small organic molecules and inorganic salt solutions. The inorganic salt retention rate was analyzed using SPSS software, and the results indicated excellent membrane stability. In summary, the preparation of PVDF/PDA–GO–TFN membrane materials provides a novel approach for fabricating LNF membranes that can effectively separate small organic molecules and inorganic salts.

Inorganic Salt Solution Assisted Grinding Synthesis of Stimuli-Responsive Perovskites for Reversible Information Encryption and Decryption Based on I Ching 64 Hexagrams

Inorganic Salt Solution Assisted Grinding Synthesis of Stimuli-Responsive Perovskites for Reversible Information Encryption and Decryption Based on I Ching 64 Hexagrams

Electrode wettability and capacitance of electrical double layer capacitor: a classical density functional theory study

We suggest a coarse-grained water model for use in classical density functional theory (cDFT) to describe aqueous inorganic salt solutions that act as working electrolytes in electrical double-layer capacitors (EDLCs) with electrodes comprising two face-to-face doped carbon monolayers. Focus of the cDFT calculations lies on the influence of solvent electrode wettability (SEW) on capacitance and energy storage behaviors, while also considering its interaction with factors like electrolyte bulk concentration, pore size, electrode voltage, and temperature. New phenomena are disclosed theoretically. Remarkably, this study challenges the traditional notion that energy storage is consistently boosted by enhancing the electrode’s ionophobicity. Contrarily, the SEW effect reduces energy storage below the standard aqueous electrochemical window voltage (around 1.2 V) and only enhances the energy storage as the voltage surpasses a certain threshold up to the optimal window voltage (2 V–2.5 V). Furthermore, a non-monotonic SEW effect on energy storage is demonstrated under appropriate conditions, shedding new light on the complex relationship between ionophobicity and energy storage. Moreover, the present coarse-grained water model enables the prediction of the experimentally observed inverse relationship between temperature and capacitance. In contrast, the widely used electrolyte primitive model predicts the existence of a maximum value. The decisive factor for the impact of SEW on capacitance and energy storage is identified as congestion within the electrode pore, while other factors contribute by affecting this congestion. The present research offers valuable insights, highlighting the significance of SEW in the innovative and strategic design of aqueous inorganic EDLC devices.

Разработка технологии регенерации некондиционных эмульсионных полуфабрикатов промышленных взрывчатых веществ

The research is aimed at improving the methods to produce and apply in the mining industry energy-intensive emulsions based on concentrated solutions of inorganic salts (nitrates), which are second-class dispersions of the "Water-inOil" type. Every year when mining useful minerals, surface and underground operations consume about 1.15 million tonnes of industrial emulsion explosives (IEE), the largest share of which are the so-called caseless pouring types. When the emulsion matrix is produced, it is possible that off-grade emulsion, i.e. emulsion that does not meet the requirements of the relevant normative and technical documentation, may also be generated. Tentatively, the volume of such production waste may reach 57.5 thousand tonnes per year. Therefore, the issues of reclaiming the off-grade emulsion semi-finished products of industrial explosives into initial products for their reuse is not only of scientific and technical interest, but also of great economic and ecological importance. The objective of this study, performed by employees of AZOTTECH LLC in cooperation with the D. I. Mendeleev Russian University of Chemical Technology, is the development of a method and industrial technology to recycle emulsion production wastes for re-use of the reclaimed materials in production. A chemical method of controlled emulsion destruction was obtained based on the results of the performed research activities. The most effective demulsifier available in the Russian market was selected, by means of which it was possible to separate the emulsion into immiscible phases containing the initial components. Samples of the stable emulsion matrix that match the requirements of the normative documents in terms of quality, were obtained using the oil phase reclaimed materials and the oxidant solution.

Study on the effects of inorganic salts and ionic surfactants on the wettability of coal based on the experimental and molecular dynamics investigations

Through the evaluation and preparation of a novel inorganic salt composite solution consisting of sodium dodecyl benzene sulfonate (SDBS), the nonionic surfactants polyethylene glycol pisooctyl phenyl ether (Triton X-100), and inorganic salt Na2SO4, based on surface tension, contact angle, settling time, wetting rate, and changes in the surface microstructure and functional groups of coal, this study analyzed the wetting behavior of the solution on coal dust and its adsorption capacity on the surface of coal particles. The results demonstrate that the composite solution of inorganic salts can significantly enhance the wettability of coal samples, reducing the contact angle to 21.54° and lowering the surface tension to 26.10 mN/m. After treatment with the solution, the relative content of oxygen-containing functional groups in the microscopic structure of the coal sample increased to 59.6 % and pores more prominent than 25 nm increased to 34.63 %. Molecular dynamics (MD) simulations of the water-inorganic salt composite solution-coal system are conducted using Materials Studio software, revealing that after the addition of the composite solution, the self-diffusion coefficient (D) of water molecules is 6.3 × 10-9 m2/s, the starting point of the composite solution is 15 Å, and the system's interaction energy increase to 14000 kcal/mol. It further elucidated the modification of the surface molecular structure of coal dust by the inorganic salt composite solution, increasing hydrogen bonds, enhancing wetting, and demonstrating a solid adsorption capability of the inorganic salt composite solution on the surface of coal dust.

Identifying the regularities of n-heptane flame inhibition by inorganic compounds

The task related to using inorganic compounds for extinguishing flames is to enable their inhibitory capacity during operation within wide limits. Therefore, the object of the current research was aqueous solutions of inorganic salts, on which the effectiveness of inhibitory properties during interaction with n-heptane flame was established. It has been proven that increasing the mass flow rate of water by 1.5 mg/s reduces the intensity of OH-radicals radiation from 70 % to 30 % and lowers the flame temperature by 90 °C. However, it was found that when potassium salts are given, the intensity of OH-radicals radiation decreases by more than 6 times, potassium chloride and sulfate reduce the intensity of OH-radicals radiation by more than 2.8 times. Among ammonium salts, salts of dihydrogen phosphate and ammonium hydrogen phosphate reduce the relative intensity of radiation of OH radicals by more than 1.3 times. Sodium salts include nitrates and sodium chloride, which reduce the relative radiation intensity of OH radicals by more than 1.6 times. This is manifested, first of all, in the enrichment of the combustible environment with fuel. When determining the flame temperature of flammable liquids, it was established that n-heptane has the most stable and highest flame temperature, which is 1768 °C. When adding inorganic compounds to the flame of n-heptane, nitrate salt, and potassium chloride, the flame temperature increased by less than 20 °C. However, ammonium salts increased the flame temperature to over 140 °C, despite the presence of water. The practical significance is that the results were taken into account during the design and development of extinguishing agents for extinguishing fires. Therefore, there are reasons to assert the possibility of regulating flame extinguishing processes by using inorganic compounds capable of inhibiting active flame radicals

Hubungan Lingkungan Sosial, Pengetahuan Ibu, Dan Status Gizi Terhadap Produksi ASI Pada Ibu Nifas Di Rumah Sakit Firdaus Jakarta Utara

Introduction: Mother's Milk (ASI) is an emulsion of fat in a solution of protein, lactose, and inorganic salts secreted by the mother's mammary glands and is useful as baby food. Breast milk production is the process of forming breast milk which involves the hormone prolactin and the hormone oxytocin. The purpose of this study was to determine the relationship between social environment, mother's knowledge, and nutritional status on breast milk production in post-partum mothers at Firdaus Hospital, North Jakarta in 2023. Methods: The design of this study was an analytic descriptive quantitative method with a cross-sectional approach with a total sample of 52 mothers. Post-partum who conducted an examination at Firdaus Hospital, North Jakarta. Results: The results of the chi-square statistical test showed that there was a relationship between social environment (p-value 0,011); mother's knowledge (p-value 0,011) and nutritional status (p-value 0,000) with milk production in post-partum mothers. Discussion: The conclusion in this study is that there is a significant relationship between the social environment, mother's knowledge and nutritional status on the production of breast milk in post-partum mothers at Firdaus Hospital, North Jakarta in 2023. Suggestions for post-partum mothers to be able to improve their nutritional fulfillment during the breastfeeding period by implementing good and correct eating patterns in accordance with the nutritional adequacy rates recommended by health workers.

In English

Currently, textile and food industries produce a significant volume of sewages containing azo dyes and other organic pollutants. These effluents are serious environmental threats, so new methods for their treatment and the degradation of azo dyes are attracting much attention. Composite materials based on TiO2 modified by noble metals and nanoceria show high activity in the photodegradation of organic contaminates and are proposed for hydrogen synthesis as well. To optimize the treatment of contaminants, different processes can combine including the strategies of adsorption, photoluminescence, photocatalysis, etc. The synthesized TiO2-based nanomaterials (sols, powders) will be exploited for bioremediation due to their small size and surface plasmon resonance from noble metals. Binary nanocomposites based on TiO2 were obtained by the chemical co-precipitation method from solutions of titanium tetraisopropoxide (TTIP) and inorganic salts of cerium, silver, and palladium. It has been stated that TiO2 is represented by anatase with primary particle size (CSR) from 8.5 to 16.8 nm, depending on the nature and concentration of the dopant. It is shown that Ag is reduced on the surface of anatase particles and blocks their growth, while Pd and Ce penetrate the titanium dioxide matrix in the form of small clusters with the deformation of the anatase crystal lattice. Nanocomposite particles formed loose and fragile aggregates, which spontaneously dispersed in solutions of dyes with the formation of colloid-stable sols, required the use of a centrifugal field for their sedimentation. Nanoparticles of TiO2&Pd were electronegative and others were electropositive according to the values 4.1÷9.6 of ZPC (zero point of charge). It was shown that the particles of all composites sorbed Methylene Blue (MB) without photocatalytic activity under the visible light to any dye. Moreover, anionic dyes such as Orange-G (Or-G) and Methyl Orange (MO) were excellently discolorated in the presence of TiO2&Pd system; cationic dyes of MB and Rhodamine B (RhB) discolorated too with the TiO2, TiO2&CeO2, and TiO2&Ag systems under UV light action. As such, photocatalysis tests showed that Orange-G’s and MO’s discoloration was higher for TiO2&Pd (2 wt. %) and TiO2 systems with the correlation coefficient R2 0.999.

Preparation of cellulose-paraffin composite foams by an emulsion–gelation method using aqueous inorganic salt solution for thermal energy regulation

Leakage of paraffin phase-change materials during phase transitions limits their application. Cellulose is an environment-friendly material that has the potential to resolve leakage problems. In this study, large-scale, firm, and no leakage cellulose-paraffin composite foams were fabricated via an emulsion–gelation method using a cellulose/LiBr solution. Spherical paraffin particles were embedded into the three-dimensional nanofibrillar network structure of the regenerated cellulose, with no chemical interaction between the paraffin and cellulose. This cellulose-paraffin foam exhibited excellent mechanical properties, with a maximum elastic modulus value of 7.08 MPa. No leakage was observed at 80 °C even when the paraffin content was 80 %. During phase change, the maximum latent heat was 173.2 J g−1. The thermal conductivity was relatively low (46.5–77.2 mW m−1); this represented 23–38 % of the thermal conductivity of pure paraffin. Therefore, foams are promising materials for efficient and reliable thermal energy storage applications.

Structures and bonding characteristics of KCl(H2O)n clusters with n = 1-10 based on density functional theory.

Aqueous inorganic salt solutions play a prominent role in both physiological and chemical experiments, and significant attention has been directed toward understanding the mechanisms underlying salt dissolution. In our effort to elucidate the hydration process of potassium chloride, we employed a comprehensive genetic algorithm to explore the structures of KCl(H2O)n (n = 1-10). A series of stable structures were identified by high-level abinitio optimization and single-point energy calculations with a zero-point energy correction. An analysis of the probability distribution of KCl(H2O)1-10 revealed that clusters with high probability at low temperatures exhibit reduced probabilities at higher temperatures, while others become more prevalent. When n = 1-9, the contact ion pair configurations or partially dissociated structures dominate in the system, and the probability distribution plot shows that the proportion of the solvent-separated ion pair (SSIP) structures of KCl(H2O)n is very small, while the SSIP configuration in KCl(H2O)10 becomes a stable structure with increasing temperature. The results from natural bond orbital analysis reveal a stronger interaction between chloride ions and water molecules. These findings provide valuable insights for a more comprehensive understanding of the intricacies of potassium chloride dissolution in water.

Elucidation of the Specific Ion Effects and Intermediate Structures of Cellulose Fibers Swollen in Inorganic Salt Solutions via In Situ X-ray Diffraction.

The solubilities of many substances are significantly affected by specific ions, as demonstrated by the Hofmeister series of proteins. Cellulose has a resistant fibrillar structure that hinders its swelling and dissolution. Certain inorganic salt solutions are effective swelling agents and solvents for cellulose. However, the precise effects of these ions on cellulose are not fully understood. In this study, we studied the intermediate structures of cellulose fibers during their swelling process in ZnCl2 and LiBr solutions via in situ X-ray diffraction. Two swollen phases with characteristic morphologies were observed for both salt treatments. Only the surfaces of the fibers were swollen in ZnCl2, whereas the ions penetrated the fibers and formed complexes with cellulose while the morphology of the fibers was maintained in LiBr. Our findings clarify the reasons that ZnCl2 has been used as an excellent swelling agent, whereas LiBr has been used as a good solvent for cellulose.

Enhanced electrochemical discharge of Li-ion batteries for safe recycling.

The recycling of spent lithium-ion batteries (LIBs) is crucial to sustainably manage resources and protect the environment as the use of portable electronics and electric vehicles (EVs) increases. However, the safe recycling of spent LIBs is challenging, as they often contain residual energy. Left untreated, this can trigger a thermal runaway and result in disasters during the recycling process. For efficient recycling, it is important to withdraw any leftover energy from LIBs, regardless of the processing method that follows the discharge. The electrochemical discharge method is a quick and inexpensive method to eliminate this hazard. This method works by immersing batteries in an aqueous inorganic salt solution to discharge LIBs completely and efficiently. Previously, research focus has been on different inorganic salt solutions that release toxic or flammable gaseous products during discharge. In contrast, we present an entirely new approach for electrochemical discharge - the utilization of an Fe(ii)-Fe(iii) redox couple electrolyte. We show that this medium can be used for efficient LIB deep discharge to a voltage of 2.0 V after rebound, a level that is low enough for safe discharge. To accomplish this, periodic discharge methods were used. In addition, no corrosion on the battery casing was observed. The pH behavior at the poles was also investigated, and it was found that without convection, gas evolution during discharge cannot be avoided. Finally, it was discovered that the battery casing material plays a vital role in electrochemical discharge, and its industrial standardization would facilitate efficient recycling.

Исследования поверхностной и адсорбционной активности модифицированного лигносульфонатного реагента для регулирования параметров бурового раствора

The possibility of obtaining a modified lignosulfonate reagent based on acrylic and lignosulfonate components is considered. To study the effect of electrolytes on the surface activity of a complex reagent based on acrylic and lignosulfonate components, the surface tension of aqueous solutions of inorganic salts of NaCl and CaCl2 of different concentrations was determinedwith the introduction of 0.1 to 2% of the reagent. The assessment of adsorption activity was carried out on the basis of constructingan isotherm of surface tension at the liquid-liquid interface under static conditions in time at a constant concentrationof the reagent. The possibility of a modified lignosulfonate reagent to effectively reduce the conditional viscosity of clay drilling mud in the temperature range from 20 to 180°C has been established.

Volumetric and acoustical properties of dextrose in aqueous solution of inorganic salts (NaCl/KCl) at various temperatures using ultrasonic tactic

Volumetric and acoustical properties of dextrose in aqueous solution of inorganic salts (NaCl/KCl) at various temperatures using ultrasonic tactic

Effect of inorganic cation on dynamic characteristics of bubble generation

Understanding the effect of inorganic cations on dynamic bubble generation is an important precursor for predicting the bubble characteristics in actual coal flotation. Using the high-speed motion acquisition system, we investigated the bubble growth in different inorganic salt solutions. The bubble generation process was divided into Formation, Expansion, and Contraction stages according to the contact angle between the bubble and the capillary as 90°. Na+, Mg2+, Ca2+, and Al3+ were found to promote bubble growth during the Formation and Expansion stages while restraining the growth during the Contraction stage. Al3+ roughly presented the most obvious promotion of the bubble generation. The dynamic bubble width and length during different bubble growth stages were analyzed to discuss the bubble pressure. The internal pressure increased as the bubble grew. The pressure difference inside and outside the bubble generally followed the order Na+ > Mg2+ > Ca2+ > Al3+. The forces acting on the bubble were attempted to be discussed. The net force acting on the bubble first kept constant and then decreased with the concentrations of Na+, Mg2+, and Ca2+, while it first decreased and then increased in the presence of Al3+. Our results can provide valuable insight into the development of the technology for mineral flotation.

Effectiveness of breast acupressure towards increasing breastmilk production in postpartum mothers

Breast Milk is an emulsion of fat in a solution of protein, lactose and inorganic salts secreted by the mammary glands which is useful as baby food. According to the 2019 Indonesian Health Demographic Survey, the achievement of exclusive breastfeeding in Indonesia was 61.33%, but not all babies were breastfed on the first day until the third day. Efforts to increase breast milk production can be done through pharmacology and non-pharmacological therapies. Pharmacological therapy can be performed by consuming breast-feeding drugs, non-pharmacological therapy can be performed by providing breast acupressure. This study aim to find out the intervention procedures, the benefits of breast acupressure intervention on the increase in breast milk production. This was a systematic literature review. Literature searching conducted for articles used electronic databases of Science Direct, Pubmed, Google Scholar, and Scopus. Articles that met the inclusion criteria were further analyzed systematically. Based on the systematic review on 10 selected article, it was explained that breast acupressure could help increase breast milk production among postpartum women. Breast acupressure could help increase breast milk production among postpartum women.

Consolidation and Compressibility Behavior of Compacted Nanoclay-Amended Bentonite Liners Inundated with Inorganic Salt Solutions

Consolidation and Compressibility Behavior of Compacted Nanoclay-Amended Bentonite Liners Inundated with Inorganic Salt Solutions