Chloride Concentration Research Articles

Synthesis of Mesoporous Silica Sol with Low Refractive Properties for Increasing Transmittance

Currently, coating with anti-reflective materials is an attractive approach to improve the quality of screen-based displays. In this study, mesoporous silica particles were systematically synthesized as a function of surfactant (i.e., CTAC-cetyltrimethylammonium chloride) concentration to serve as main coating fillers possessing low refractive indices. Precisely changing the amount of the CTAC surfactant, silica sol with an average diameter of 50 nm exhibits distinctively different specific surface areas, pore size, and pore volume. Prior to the preparation of final coating solutions containing these silica particle fillers, the percentage of solid content was optimized on a glass slide. The use of 50 wt% solid content exhibited the highest transmittance of light. Among various content levels of silica sol, the use of 3.5 wt% of silica particles in the solid content displayed the highest transmittance (i.e., best anti-reflectiveness). Under the almost identical coating layers prepared with the fixed amount of silica particles possessing different surface areas, pore size, and pore volume, it appears that the largest pore volume played the most important role in improving the anti-reflective properties. Experimentally understanding the key feature of low-refractive filler materials under the optimized conditions could provide a clear view to develop highly effective anti-reflective materials for various display applications.

Chloride Gradient Is Involved in Ammonium Influx in Human Erythrocytes

The ammonia/ammonium (NH3/NH4+, AM) concentration in human erythrocytes (RBCs) is significantly higher than in plasma. Two main possible mechanisms for AM transport, including simple and facilitated diffusion, are described; however, the driving force for AM transport is not yet fully characterized. Since the erythroid ammonium channel RhAG forms a structural unit with anion exchanger 1 (eAE1) within the ankyrin core complex, we hypothesized the involvement of eAE1 in AM transport. To evaluate the functional interaction between eAE1 and RhAG, we used a unique feature of RBCs to swell and lyse in isotonic NH4+ buffer. The kinetics of cell swelling and lysis were analyzed by flow cytometry and an original laser diffraction method, adapted for accurate volume sensing. The eAE1 role was revealed according to (i) the changes in cell swelling and lysis kinetics, and (ii) changes in intracellular pH, triggered by eAE1 inhibition or the modulation of eAE1 main ligand concentrations (Cl− and HCO3−). Additionally, the AM import kinetics was analyzed enzymatically and colorimetrically. In NH4+ buffer, RBCs concentration-dependently swelled and lysed when [NH4+] exceeded 100 mM. Cell swelling and hemolysis were tightly regulated by chloride concentration. The complete substitution of chloride with glutamate prevented NH4+-induced cell swelling and hemolysis, and the restoration of [Cl−] dose-dependently amplified the rates of RBC swelling and lysis and the percentage of hemolyzed cells. Similarly, eAE1 inhibition impeded cell swelling and completely prevented hemolysis. Accordingly, eAE1 inhibition, or a lack of chloride anions in the buffer, significantly decreased NH4+ import. Our data indicate that the eAE1-mediated chloride gradient is required for AM transport. Taken together, our data reveal a new player in AM transport in RBCs.

Establishment of a conditionally reprogrammed primary eccrine sweat gland culture for evaluation of tissue-specific CFTR function

BackgroundSweat chloride concentration is used both for CF diagnosis and for tracking CFTR modulator efficacy over time, but the relationship between sweat chloride and lung health is heterogeneous and informed by CFTR genotype. Here, we endeavored to characterize ion transport in eccrine sweat glands (ESGs). MethodsFirst, ESGs were microdissected from a non-CF skin donor to analyze individual glands. We established primary cultures of ESG cells via conditional reprogramming for functional testing of ion transport by short circuit current measurement and examined cell composition by single-cell RNA-sequencing (scRNA-seq) comparing with whole dissociated ESGs. Secondly, we cultured nasal epithelial (NE) cells and ESGs from two people with CF (pwCF) to assess modulator efficacy. Finally, NEs and ESGs were grown from one person with the CFTR genotype F312del/F508del to explore genotype-phenotype heterogeneity. ResultsESG primary cells from individuals without CF demonstrated robust ENaC and CFTR function. scRNA-seq demonstrated both secretory and ductal ESG markers in cultured ESG cells. In both NEs and ESGs from pwCF homozygous for F508del, minimal baseline CFTR function was observed, and treatment with CFTR modulators significantly enhanced function. Notably, NEs from an individual bearing F312del/F508del exhibited significant baseline CFTR function, whereas ESGs from the same person displayed minimal CFTR function, consistent with observed phenotype. ConclusionsThis study has established a novel primary culture technique for ESGs that allows for functional ion transport measurement to assess modulator efficacy and evaluate genotype-phenoytpe heterogeneity. To our knowledge, this is the first reported application of conditional reprogramming and scRNA-seq of microdissected ESGs.

Mapping and assessment of groundwater pollution risks in the main aquifer of the Mostaganem plateau (Northwest Algeria): utilizing the novel vulnerability index and decision tree model.

Water plays a pivotal role in socio-economic development in Algeria. However, the overexploitations of groundwater resources, water scarcity, and the proliferation of pollution sources (including industrial and urban effluents, untreated landfills, and chemical fertilizers, etc.) have resulted in substantial groundwater contamination. Preserving water irrigation quality has thus become a primary priority, capturing the attention of both scientists and local authorities. The current study introduces an innovative method to mapping contamination risks, integrating vulnerability assessments, land use patterns (as a sources of pollution), and groundwater overexploitation (represented by the waterhole density) through the implementation of a decision tree model. The resulting risk map illustrates the probability of contamination occurrence in the substantial aquifer on the plateau of Mostaganem. An agricultural region characterized by the intensive nutrients and pesticides use, the significant presence of septic tanks, widespread illegal dumping, and a technical landfill not compliant with environmental standards. The critical situation in the region is exacerbated by excessive groundwater pumping surpassing the aquifer's natural replenishment capacity (with 115 boreholes and 6345 operational wells), especially in a semi-arid climate featuring limited water resources and frequent drought. Vulnerability was evaluated using the DRFTID method, a derivative of the DRASTIC model, considering parameters such as depth to groundwater, recharge, fracture density, slope, nature of the unsaturated zone, and the drainage density. All these parameters are combined with analyses of inter-parameter relationship effects. The results show a spatial distribution into three risk levels (low, medium, and high), with 31.5% designated as high risk, and 56% as medium risk. The validation of this mapping relies on the assessment of physicochemical analyses in samples collected between 2010 and 2020. The results indicate elevated groundwater contamination levels in samples. Chloride exceeded acceptable levels by 100%, nitrate by 71%, calcium by 50%, and sodium by 42%. These elevated concentrations impact electrical conductivity, resulting in highly mineralized water attributed to anthropogenic agricultural pollution and septic tank discharges. High-risk zones align with areas exhibiting elevated nitrate and chloride concentrations. This model, deemed satisfactory, significantly enhances the sustainable management of water resources and irrigated land across various areas. In the long term, it would be beneficial to refine "vulnerability and risk" models by integrating detailed data on land use, groundwater exploitation, and hydrogeological and hydrochemical characteristics. This approach could improve vulnerability accuracy and pollution risk maps, particularly through detailed local data availability. It is also crucial that public authorities support these initiatives by adapting them to local geographical and climatic specificities on a regional and national scale. Finally, these studies have the potential to foster sustainable development at different geographical levels.

Analytically monitored cultivation of Arthrospira platensis on food waste extracts to compose a sustainable, low-prized, Zarrouk-based medium

ABSTRACT A sustainable, low-cost medium based on food waste for cultivating the cyanobacterium Arthrospira platensis (A. platensis) was investigated. Zarrouk medium components, especially phosphate, were substituted with extracts from beetroot peel, brewer’s grains, and walnut press cake. Ion concentrations of magnesium, calcium, iron, potassium, sodium, phos-phate, nitrate, sulfate, and chloride were analyzed to determine the optimal medium composition. Walnut press cake and brewer’s grains extracts showed high potential due to their magnesium, calcium, and phosphate content. Brewer’s grains extracts also provided glucose as an additional carbon source. Cultivations in shaking flasks and a photobioreactor (PBR) monitored cell growth through optical density and biomass concentration. The excess of magnesium and reduced phos-phate concentrations positively affected biomass production. A. platensis’s ability to metabolize glucose resulted in 68% higher biomass production. Growth in brewer’s grains extract required no additional phosphate. PBR cultivation showed A. platensis consumed significant magnesium and nitrate, achieving higher biomass concentrations with optimized gas exchange and light reflection systems.

Copper leaching from complex chalcopyrite-rich ores: Utilizing mechanical activation and wastewater-based sulfuric acid system

Complex chalcopyrite-rich ore is crucial in global copper resources, but is highly refractory in conventional sulfate leaching system. In this paper, we explore the leaching of complex chalcopyrite-rich ores employing a mechanically activated pretreatment combined with wastewater with high concentrations of chloride. The investigation delves into various parameters, including reaction temperature (60 to 90 °C), sulfuric acid concentration (0.005 to 2.0 M), chloride concentration (0 to 1.5 M), liquid/solid ratio (0 to 200), stirring speed (100 to 580 rpm), leaching time (0 to 4 h) and grinding time (0 to 7 h), to evaluate their impact on copper recovery from complex chalcopyrite-rich ores. Furthermore, a comprehensive kinetic analysis of copper leaching behavior was studied, encompassing specific surface area, amorphization degree, grain size, and microstrain. In the sulfuric acid system utilizing wastewater, the presence of mechanical activation and chloride content enhances copper leaching while mitigating the passivating effect of elemental sulfur. Notably, following a leaching period of 4 h at 80 °C, the copper leaching efficiency remarkably reached 89.46 %. In addition, kinetic analysis of copper leaching at temperatures ranging from 60 to 90 °C via a shrinking core model with R2 > 97 %, indicates that the leaching process of copper is primarily governed by solid product layer diffusion, with an activation energy of 54.32 kJ/mol. These findings highlight the efficacy of the proposed approach in optimizing copper recovery from complex chalcopyrite-rich ores, offering insights into the underlying mechanisms driving the leaching process.

Ionic strength effect on the structure and dynamics of colloidal dispersions with weak attractive interactions

We present a macro- and microrheological study of the effect of ionic strength on the phase behavior, structure and flow properties of colloidal dispersions stabilized by short-range repulsive interactions inferred via co-polymerization of weak acid groups. We investigated the impact of ionic strength, by varying the concentration of natrium chloride (NaCl), on dispersions with only repulsive interactions, but also when additional attractive depletion forces are present due to added non-absorbent polymer, namely polyethyleneoxide (PEO). For dispersions with only repulsive electrosteric interactions, at low particle volume fractions (ϕ < 0.4), increasing ionic strength hardly affects the relative viscosity whereas at higher particle volume fractions, a decrease in viscosity is observed due to a reduced range of electrosteric repulsion between particles, corresponding to a reduction of the effective particle volume fraction ϕeff.For dispersions including attractive interactions, at volume fractions ϕ = 0.45 below the hard sphere freezing point (ϕc=0.5), independently of the ionic strength, the bulk viscosity increases monotonically with increasing PEO concentration due to the transition from a fluid to a fluid/crystalline and finally to a gel state. However, the increase in ionic strength shifts the concentrations of both phase transitions to lower polymer concentrations, indicating that in presence of salt a weaker attraction is required to induce these transitions. At ϕ=0.52, just above ϕc, for dispersions without added salt, broadening of the fluid-crystalline coexistence regime, due to added PEO, results in a viscosity minimum corresponding to different size and packing density of the crystalline regions as observed earlier in Weis et al. [1]. When salt is added, the initial state for dispersions without PEO is a fluid state due to the reduction of ϕeff and the addition of a small amount of PEO leads to an increase in bulk viscosity due to the formation of large crystals for dispersions containing 10mM NaCl and a network of small, dense crystals of size ≈10µm when 100mM NaCl is added.At ϕ=0.54, a result similar to ϕ=0.52 is obtained for dispersions without added salt, whereas in presence of salt, we find that the fluid/crystalline coexistence regime narrows down as the range of electrosteric repulsion decreases and the addition of PEO results in gel formation and gels become more uniform with increasing attraction strength. These investigations demonstrate how superimposed short range electrosteric repulsion and weak depletion attraction affect microstructure and flow behavior of colloidal dispersions.

Mechanism and rate of anomalous extraction of chloride salts from water to 1,2-dichloroethane

Open circuit potential (OCP) measurements, potentiostatic pulse (PP) amperometry and cyclic voltammetry (CV), were used to investigate and to sort by rate the anomalous extraction of the chloride salts RCl of the cations R+ = tetrabutylammonium (TBA+), tetrapentylammonium (TPeA+), tetrahexylammonium (THexA+), tetraheptylammonium (THepA+) and bis(triphenyl-phosphoranylidene)ammonium (BA+) from water to 1,2-dichloroethane (DCE). A tentative mechanism is proposed comprising (a) the diffusion-controlled transport of the ion-pairs (RCl)ip from the aqueous to the organic solvent phase providing a major contribution to the chloride extraction, (b) decomposition of the multiple ion-pairs or clusters (RCl)ipx, which are formed by agglomeration of the single ion-pairs (RCl)ip in the aqueous phase (w), and (c) the exponential decay of the ion-pairs (RCl)ip accumulated on the organic solvent side of the interface at the beginning of the OCP measurements. This model enables to simulate successfully the experimental time dependence of the chloride concentration. A conclusion is made that the effect of the composition of the organic solvent electrolyte RX, where X- = tetraphenylborate (TPB-) or tetrakis(pentafluorophenyl) borate (TB-), on the rate and extent of the anomalous accumulation of the chloride anion in the phase (o) of the two-phase liquid system LiCl(w)/RX(o) can be related to the hydrophobicity of the electrolytes RCl and RX. The latter property can be characterized by the standard Gibbs energy of transfer from the aqueous (w) to the organic solvent (o) phase. The accumulation of the chloride anion in the phase (o) appears to be promoted by the decreasing value of the transfer Gibbs energy of RCl in the sequence TBACl > TPeACl > THexACl > THepACl > BACl, while the decreasing value of the transfer Gibbs energy of RX in the sequence TBATPB > TPeATPB > THexATPB > THepATPB > BATPB > BATB starts to block the cycle combining the energetically unfavorable extraction of RX from the phase (o) to the phase (w) with the energetically favorable extraction of RCl in the opposite direction. IR spectroscopy provides evidence of the formation of the water clusters in the organic solvent phase equilibrated with the aqueous phase in the presence of the tetraalkylammonium cation in both phases, which are supposed to drive the anomalous accumulation of the chloride anion in the phase (o).

Focusing on the corrosion resistance enhancement of HRB400 rebar by Cr addition in the marine envrionment

The corrosion resistance of Cr reinforced HRB400 rebar in the marine environment was investigated. The addition of Cr increases the amount of Cr(OH)3 and α-FeOOH in the passivate film, resulting in a denser passivate film structure. This enhanced passivation film inhibits localized corrosion. The pitting potential and critical chloride concentration (CTL) of the steel increased with the increase in chromium content, indicating improved corrosion resistance of the steel. On the other hand, an increase in the concentration of Cl- in solution leads to a decrease in the pitting potential and resistance of the steel, which reduces the corrosion resistance. At higher Cl- concentrations, the Cl- ions form an electrochemical interface with the steel surface, resulting in a sharp decrease in the Rf value. In addition, the gradual decrease in solution pH leads to a decrease in the pitting potential and CTL of HRB400 and 1.5Cr steel. The corrosion resistance was also found to be reduced, pH reduction accelerated the intrusion of chloride ions, which led to a severe breakdown of the passivation film.

Mechanical performance and permeability of low-carbon printable concrete

Common issues in 3D printed concrete arise due to its high cement content, processing requirements, and the lack of extensive research into its long-term performance. To this end, this study explores using supplementary cementitious materials from local regions to partially replace cement, aiming at reducing the carbon footprint. Various printable mixtures with different substitution rates are formulated, and corresponding mechanical and permeability tests are conducted. It is revealed that the compressive and flexural strengths of 3D printed concrete with low cement content were lower than the strength of cast concrete due to the construction process of printed concrete; the mechanical strength of 3D printed concrete showed prominent anisotropic characteristics. It was found that, compared with the other two sets of ratios, the higher contents of FA and GGBFS could effectively fill the pores of the printed concrete. Both the capillary water absorption and the content of chloride ions of the low-carbon mixture were significantly lower than that of the pure cement-printed specimens.

A three-phase model based on boundary element method for simulation of chloride diffusion in concrete

Chloride-induced corrosion of steel reinforcements has been identified as one of the main causes of deterioration of concrete structures. A feasible numerical method is required to predict chloride penetration in concrete structures. In this study, a three-phase model of concrete based on the Boundary Element Method (BEM) is proposed to investigate the diffusion and distribution behavior of chlorides in concrete. Compared with the finite element model (FEM), the proposed model has a higher computational efficiency, and a comparison of the simulated chloride concentration with the corresponding experimental data is proved to be reasonable. Furthermore, the parametric analysis is carried out to evaluate the effect of coarse aggregate parameters on chloride diffusion in concrete. The results show that chloride attack was more susceptible to the coarse aggregate content and less affected by the ITZ diffusion coefficient. This may be due to the fact that the volume fraction of aggregates in concrete is much higher than that in the ITZ. In addition, the low permeability of the coarse aggregate hindered the diffusion of chloride ions, while the ITZ around the aggregate accelerated the diffusion of chloride ions. when the aggregate content increases in a certain range from 12.56 % to 50.24 %, the hindering effect of aggregate on chloride ion diffusion is more obvious than the accelerating effect of ITZ.

Изменение активности оксидоредуктаз чернозема обыкновенного при загрязнении платиной

The automotive industry is the main source of environmental pollution with platinum group metals, which increases the concentration of platinum in road dust, soil, and plants. This can lead to the achievement of toxic levels of this metal in the environment, and consequently, an imbalance of the ecosystem, a reduction in the microbial population, and a decrease in soil fertility. The effects of platinum on the activity of oxidoreductases of ordinary chernozem have been studied: the activity of catalase and dehydrogenase. Platinum was introduced into the soil in the form of chloride. Platinum concentrations were studied – 0.01; 0.1; 1; 10 and 100 mg/kg. The change in the indicators of ordinary chernozem was assessed 10, 30 and 90 days after contamination. The absence of a stimulating effect of platinum chloride on catalase activity, the effect of hormesis on the activity of dehydrogenases of ordinary chernozem has been established. The dependence of the degree of decrease in indicators on the concentration of the pollutant in the soil and the time from the moment of contamination is shown. The study shows the negative effect of even a small concentration (0.1 mg/kg) of platinum chloride on the enzymatic activity of the soil. Early diagnosis of the degree of soil contamination with platinum compounds can be successfully used to promptly assess their impact on soil condition and prevent possible negative consequences.

Isolation, molecular identification, and genomic analysis of Mangrovibacter phragmitis strain ASIOC01 from activated sludge harboring the bioremediation prowess of glycerol and organic pollutants in high-salinity.

The physiological and genotypic characteristics of Mangrovibacter (MGB) remain largely unexplored, including their distribution and abundance within ecosystems. M. phragmitis (MPH) ASIOC01 was successfully isolated from activated sludge (AS), which was pre-enriched by adding 1,3-dichloro-2-propanol and 3-chloro-1,2-propanediol as carbon sources. The new isolate, MPH ASIOC01, exhibited resilience in a medium containing sodium chloride concentration up to 11% (with optimal growth observed at 3%) and effectively utilizing glycerol as their sole carbon source. However, species delimitation of MGBs remains challenging due to high 16S rRNA sequence similarity (greater than 99% ANI) among different MGBs. In contrast, among the housekeeping gene discrepancies, the tryptophan synthase beta chain gene can serve as a robust marker for fast species delimitation among MGBs. Furthermore, the complete genome of MPH ASIOC01 was fully sequenced and circlized as a single contig using the PacBio HiFi sequencing method. Comparative genomics revealed genes potentially associated with various phenotypic features of MGBs, such as nitrogen-fixing, phosphate-solubilizing, cellulose-digesting, Cr-reducing, and salt tolerance. Computational analysis suggested that MPH ASIOC01 may have undergone horizontal gene transfer events, possibly contributing unique traits such as antibiotic resistance. Finally, our findings also disclosed that the introduction of MPH ASIOC01 into AS can assist in the remediation of wastewater chemical oxygen demand, which was evaluated using gas chromatograph-mass spectrometry. To the best of our knowledge, this study offers the most comprehensive understanding of the phenotypic and genotypic features of MGBs to date.

Fluid resuscitation with balanced electrolyte solutions results in faster resolution of diabetic ketoacidosis than with 0.9% saline in adults – A systematic review and meta‐analysis

AbstractFluid resuscitation during diabetic ketoacidosis (DKA) is most frequently performed with 0.9% saline despite its high chloride and sodium concentration. Balanced Electrolyte Solutions (BES) may prove a more physiological alternative, but convincing evidence is missing. We aimed to compare the efficacy of 0.9% saline to BES in DKA management. MEDLINE, Cochrane Library, and Embase databases were searched for relevant studies using predefined keywords (from inception to 27 November 2021). Relevant studies were those in which 0.9% saline (Saline‐group) was compared to BES (BES‐group) in adults admitted with DKA. Two reviewers independently extracted data and assessed the risk of bias. The primary outcome was time to DKA resolution (defined by each study individually), while the main secondary outcomes were changes in laboratory values, duration of insulin infusion, and mortality. We included seven randomized controlled trials and three observational studies with 1006 participants. The primary outcome was reported for 316 patients, and we found that BES resolves DKA faster than 0.9% saline with a mean difference (MD) of −5.36 [95% CI: −10.46, −0.26] hours. Post‐resuscitation chloride (MD: −4.26 [−6.97, −1.54] mmoL/L) and sodium (MD: −1.38 [−2.14, −0.62] mmoL/L) levels were significantly lower. In contrast, levels of post‐resuscitation bicarbonate (MD: 1.82 [0.75, 2.89] mmoL/L) were significantly elevated in the BES‐group compared to the Saline‐group. There was no statistically significant difference between the groups regarding the duration of parenteral insulin administration (MD: 0.16 [−3.03, 3.35] hours) or mortality (OR: −0.67 [0.12, 3.68]). Studies showed some concern or a high risk of bias, and the level of evidence for most outcomes was low. This meta‐analysis indicates that the use of BES resolves DKA faster than 0.9% saline. Therefore, DKA guidelines should consider BES instead of 0.9% saline as the first choice during fluid resuscitation.

Study of corrosion resistance of superhydrophobic hydrotalcite cement mortar in chlorine salt environment

Reinforced concrete structures are susceptible to reduced service life owing to the erosion caused by the of chlorine-containing, external environment and internal chloride. In this paper, a superhydrophobic hydrotalcite cement mortar was studied with internal and external cooperation against chloride ion erosion. The effect of different hydrotalcite substitution amounts on the chlorine corrosion resistance of the mortar was investigated. The mortar exhibited good resistance to chlorine corrosion, and the corrosion resistance rate increased by 91.83 %. The free chloride ion concentration measurement and rapid chloride migration test exhibited that the prepared mortar effectively resisted chloride ion invasion and reduced the content of free chloride ions in the mortar. The proposed anticorrosion method is expected to have potential application prospects for concrete structures under chloride salt environments.

Service Life of Pre-Tensioned Concrete Structures in a Chloride Environment on the Example of an Aluminium Foundry Building.

This paper describes a study of the chloride content in the concrete lagging of prestressed concrete elements of the roof structure of an aluminium foundry building. Sources of chloride pollution in industrial facilities are discussed. Methods for collecting dust deposited on the structure and sampling concrete for chloride concentration testing are presented in detail. The test methods used and the apparatus used to assess the chloride content at the thickness of concrete reinforcement lagging are presented. Investigations of the chloride content in the concrete of the reinforcement cover showed a very high concentration of chloride in the near-surface layer, depending on the location of the element in relation to the source of chloride emission into the environment. In contrast, the concrete of the deeper layers of the lagging contained very small amounts of Cl- chlorides. The results of the chloride content of the lagging concrete were plotted against the distance from the surface of the specimen and approximated by the function C(x,t) based on Fick's second law and its solution. A satisfactory fit of the course of this function to the experimental results was obtained. Based on the obtained C(x,t) function, the durability of the main structural components of an aluminium foundry industrial hall operating in a chloride environment was estimated.

In Situ Phase Separation-Induced Self-Healing Catalyst for Efficient Direct Seawater Electrolysis.

Direct seawater electrolysis technology for sustainable hydrogen production has garnered significant attention, owing to its abundant resource supply and economic potential. However, the complex composition and high chloride concentration of seawater have hindered its practical implementation. In this study, we report an in situ-synthesized dual-phase electrocatalyst (HPS-NiMo), comprising an amorphous phosphide protective outer phase and a crystalline alloy inner phase with supplementary sulfur active sites, to improve the kinetics of direct seawater electrolysis. The HPS-NiMo exhibits long-term stability, remaining stable for periods exceeding 120 h at 200 mA cm-2; moreover, it lowers the required operating voltage to ∼1.8 V in natural seawater. The chlorine chemistry, corrosion during direct natural seawater electrolysis, and mechanism behind the high-performing catalysts are discussed. We also investigated the possibility of recovering the anode precipitates, which inevitably occurs during seawater electrolysis.

Revealing the effects of amino acid, organic acid, and phytohormones on the germination of tomato seeds under salinity stress.

Salinity accumulation poses a threat to the production and productivity of economically important crops such as tomatoes (Solanum lycopersicum L.). Currently, salt tolerance breeding programs have been limited by insufficient genetic and physiological knowledge of tolerance-related traits and a lack of an efficient selection domain. For that purpose, we aimed to determine the ability of tomato cultivars to tolerate salt based on seed traits by multiple biochemical pathways. First, we tested three tomato cultivars according to their response to different sodium chloride (NaCl) concentrations (0, 6.3, 9.8, 13.0, and 15.8 dS m-1) and then we analysed their amino acids, organic acids, and phytohormones. Considering the results of germination traits, it is possible to conclude that cultivar H-2274 was more tolerant to salt stress than others. As a result, multivariate discriminant analysis including principal component analysis and two-way hierarchical clustering analyses were constructed and demonstrated that tomato cultivars were separated from each other by the amino acid, organic acid, and phytohormone contents. Considering germination traits of tomato seeds, cv. 'H-2274' was more tolerant to salinity than others depending on high proline (29 pmol µl-1) and citric acid (568 ng µl-1) assays. Biochemical variability offers a valuable tool for investigating salt tolerance mechanisms in tomatoes, and it will be appreciated to find high-tolerant tomato cultivar(s) to saline conditions. Also, the findings of this study have significant potential for practical applications in agriculture, particularly in developing salt-tolerant tomato cultivars to enhance productivity in saline environments and address socio-economic challenges.

Characterization of the Solution Properties of Sodium Dodecylsulphate Containing Alkaline–Surfactant–Polymer Flooding Media

Alkaline–surfactant–polymer (ASP) flooding by means of which alkali additives, surfactant and polymer are inserted as the same slug is one of the most favourable worldwide focuses of Chemical Enhanced Oil Recovery (cEOR) research and field trials, due to the individual synergy of the three chemical components. To develop efficient oil recovery chemicals, it is essential to fully understand the mechanism behind ASP flooding. Nonetheless, there are hardly any studies reporting a systematic characterization of the ASP process. Thus, the present paper focuses on modelling this process in a laboratory by the use of an anionic surfactant—sodium dodecyl sulphate (SDS) in alkaline–polymer media—which is composed of a commercial water-soluble polymer (Flopaam AN125SH®, SNF Floerger, Andrézieux-Bouthéon, France) and alkali compounds (NaOH and Na2CO3). The samples were characterized using rheometry, dynamic light scattering (DLS), infrared spectroscopy (IR) and measurement of inferfacial tension (IFT) between the samples and rapeseed oil. In accordance with the experimental results, surprisingly lower IFT values were recorded between the alkaline–polymer solutions and rapeseed oil than the samples which contained SDS. Increasing polymer and sodium chloride concentration caused a decrease (from 0.591 mN/m to 0.0486 mN/m) in IFT between the surfactant containing samples and rapeseed oil. The IR measurements confirmed that the surfactant was not detected in the oil phase in the absence of NaOH and Na2CO3. The effects of SDS on the viscosity of the mixtures were also investigated, as viscosity is a considerably important parameter in processes using polymers.

Electrocoagulation employing recycled aluminum electrodes for methylene blue remediation

This work focuses on the recycling of aluminum-based metal joinery waste in the context of the treatment of wastewater containing organic materials, such as dyes, by electrocoagulation (EC); aluminum scraps were used as electrodes to process synthetic solutions of the methylene blue (MB) dye. The study investigated the effect of different parameters, including pH (3, 4, 5, 7, 9, 11) current density (100, 150, 200, 250 A/m2), electrolysis time (30, 60,120 min), sodium chloride concentration (0.5, 1, 2 g/L) and the initial dye concentration (10, 20, 45, 60 mg/L) on the removal efficiency of MB. The results showed that the optimum conditions for MB removal were achieved at the original pH of the solution which is 7 using a current density of 200 A/m2 and an inter-electrode distance of 1 cm with 10 mg/L as a dye concentration and 2 g/L of electrolyte. The removal efficiency under these conditions can reach 97.81 %. An estimation was made of the electrical energy needed to attain the ideal removal, which was found to be approximately 0.97kWh/g removal dyestuff the electrode consumption was 0.13 (kgAl /g of dyestuff), with an operation cost of 0.106 ($/g of dyestuff). The study suggests that EC using only two aluminum electrodes is efficient technique for the removal of MB from synthetic wastewater. The removal of the dye was monitored by UV–visible spectroscopy and scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR) is used for the identification of the functional groups of MB in the obtained sludge by the EC process; and the aluminum electrodes surfaces, before and after treatment, were characterized by scanning electron microscopy (SEM) and Dispersive Energy Spectroscopy (EDS).