High Ionic Strength Research Articles

Oligomerization-mediated phase separation in the nucleoid-associated sensory protein H-NS is controlled by ambient cues.

H-NS, a nucleoid-associated protein (NAP) from enterobacteria, regulates gene expression by dynamically transducing environmental cues to conformational assembly and DNA binding. In this work, we show that H-NS from Escherichia coli, which can assemble into octameric and tetrameric oligomerization states, forms spontaneous micron-sized liquid-like condensates with DNA at sub-physiological concentrations in vitro. The heterotypic condensates are metastable at 298 K, partially solubilizing with time, while still retaining their liquid-like properties. The condensates display UCST-like phase behavior solubilizing at higher temperatures, but with a large decrease in droplet-assembly propensities at 310 K and at higher ionic strength. Condensate formation can be tuned in a cyclic manner between 298 and 310 K with the extent of reversibility determined by the incubation time, highlighting strong hysteresis. An engineered phospho-mimetic variant of H-NS (Y61E), which is dimeric and only weakly binds DNA, is unable to form condensates. The Y61E mutant solubilizes pre-formed H-NS condensates with DNA in a few minutes with nearly an order of magnitude speed-up in droplet dissolution at 310 K relative to 298 K, demonstrating rapid molecular transport between dilute and condensed phases. Our results establish that the oligomerization of H-NS is intrinsically tied not only to DNA binding but also its phase-separation tendencies, while showcasing the regulatable and programmable nature of heterotypic condensates formed by an archetypal NAP via multiple cues and their lifetimes.

Effect of isomeric polysaccharides on heteroaggregation of nanoplastics in high ionic strength conditions: Synergies of morphology and molecular conformation

Polysaccharides with various molecular structures and morphology may influence the aggregation kinetics of nanoplastics. This study used various characterization methods to elucidate the heteroaggregation mechanism of polystyrene nanoplastics (PSNPs) in the presence of polysaccharides (ionic strength (IS) 1-800mM NaCl and 0.01-60mM CaCl2). The results showed that under high IS, cellulose (CL) accelerated the heteroaggregation of PSNPs, and the aggregation rate of PSNPs increased by approximately 62.05%, while amylose (AM) had little effect (10.38%). Compared with AM (43.2nm), the morphology of the CL (78.4nm) gully had improved surface roughness, leading to its decisive role in the heteroaggregation of PSNPs. Quantum chemistry calculations indicated that van der Waals forces of PSNPs-CL systems (-217.28kJmol-1) were stronger than those of PSNPs-AM systems (-184.62kJmol-1) based on the subtle molecular conformation differences between CL and AM (opposite and same sides of OH groups in CL and AM, respectively). The morphology and molecular conformation of polysaccharides collaboratively controlled the heteroaggregation of PSNPs. Because the morphology of polysaccharides was based on their molecular conformation, the latter is the most critical factor. These findings provide new insights into the effects of PSNPs stability in the environment.

A one-step polyvinyl alcohol/polyacrylamide/polyacrylic acid/dimethyl sulfoxide/CaCl2 hybrid hydrogel enabling anti-fatigue, anti-freeze and anti-dehydration for wearable strain sensor

Hydrogel with fatigue resistance, freezing tolerant and dehydration resistance are peculiarly attractive in strain sensors. The hydrogel soaked in organic solvent is an effective strategy to improve freezing resistance and dehydration resistance, while this may result in poor conductivity. Moreover, ion-incorporation is considered to be the most feasible method for solving above concern, while high concentration of salt ions will result in weak mechanical properties. Therefore, the facile preparation of anti-freezing and anti-dehydration hydrogels with excellent fatigue resistance remains a challenge. Herein, a polyvinyl alcohol/polyacrylamide/polyacrylic acid/dimethyl sulfoxide/CaCl2 hybrid hydrogel was designed and fabricated through a facile one-step method to balance a variety of outstanding properties. On account of the hybridization design of multi-materials, the hybrid hydrogel exhibited high ionic conductivity (∼0.2 S/m), strength (∼0.36 MPa) and stretchability (∼825 %). Meanwhile, the hybrid hydrogel demonstrated prominent freezing resistance, dehydration resistance and fatigue resistance. The mechanical properties almost no deterioration after 1000 stretching cycle at 100 % strain, exposure to environment for 30 days or freeze at low temperature. Besides, the hybrid hydrogel-based stain sensor showed a linear sensitivity (GF = 1.12 over 0–400 % strain), quickly responsivity (200 ms), and could monitor various human activities steadily, demonstrating distinguished potential for use in wearable health monitoring and flexible electric skins.

Expression and functional study of DNA polymerases from Psychrobacillus sp. BL-248-WT-3 and FJAT-21963.

The properties of DNA polymerases isolated from thermophilic and mesophilic microorganisms, such as the thermophilic Geobacillus stearothermophilus (Bst) and mesophilic Bacillus subtilis phage (Phi29), have been widely researched. However, DNA polymerases in psychrophilic microorganisms remain poorly understood. In this study, we present for the first time the expression and functional characterization of DNA polymerases PWT-WT and FWT-WT from Psychrobacillus sp. BL-248-WT-3 and FJAT-21963. Enzymatic activity assays revealed that FWT-WT possessed strand displacement but lacked exonuclease activity and high ionic strength tolerance, whereas PWT-WT lacked all these properties. Further protein engineering and biochemical analysis identified D423 and S490 as critical mutation sites for improving strand displacement and tolerance to high ionic strength, specifically in the presence of 0-0.3 M potassium chloride (KCl), sodium chloride (NaCl), and potassium acetate (KAc). Three-dimensional structural analysis demonstrated that the size and the electric charge of the single-stranded DNA (ssDNA) encapsulation entrance were pivotal factors in the binding of the ssDNA template.

Biomass‐based crosslinked composite anion exchange membranes using bacterial cellulose template towards enhanced ionic conductivity and alkaline stability

AbstractA balanced relationship among ionic conductivity, mechanical properties and alkaline stability of anion exchange membranes (AEMs) is essential for their practical application in fuel cells. Herein, a porous substrate (BC@LDH) with hierarchical structure was constructed using natural bacterial cellulose (BC) as a template and then in situ grew inorganic hydroxide ion conductor (layered double hydroxide, LDH). The membrane was fabricated via a filling together with sol–gel crosslinking strategy after impregnating an ionomer containing both quaternary ammonium and hydroxyl groups into the porous substrate and then crosslinked by organosiloxane. Due to the synergistic enhancement effect of BC, LDH and cross‐linking, the obtained membrane exhibited a tensile strength of 47.48 MPa that was 88.3% higher than that of the pure ionomer membrane, and showed an ionic conductivity of 70.7 mS cm−1 (80°C) which benefited from the introduction of ionic conductor LDH. More importantly, its alkaline stability was significantly improved and the residual conductivity ratio was still as high as 81.5% even after hot alkali treatment for 580 h. The direct methanol fuel cell assembled with this membrane exhibited a peak power density of 13.6 mW cm−2 with an open‐circuit voltage of 0.72 V, indicating its potential application in biomass‐based AEMs for fuel cells.Highlights Hierarchical porous substrate comprising LDHs anchored BC fiber was prepared. LDH@BC served as a reinforcing substrate and an ion transport medium. The crosslinked membrane showed significantly improved alkaline stability. The membrane had high ionic conductivity and mechanical strength. Providing a new way to design biomass‐based AEMs with high performance.

Discovery of Lipoxygenase-Like Materials for Inducing Ferroptosis.

Recent research has highlighted the pivotal role of lipoxygenases in modulating ferroptosis and immune responses by catalyzing the generation of lipid peroxides. However, the limitations associated with protein enzymes, such as poor stability, low bioavailability, and high production costs, have motivated researchers to explore biomimetic materials with lipoxygenase-like activity. Here, we report the discovery of lipoxygenase-like two-dimensional (2D) MoS2nanosheets capable of catalyzing lipid peroxidation and inducing ferroptosis. The resulting catalytic products were successfully identified using mass spectrometry and a luminescent substrate. Unlike native lipoxygenases, MoS2 nanosheets exhibited exceptional catalytic activity at extreme pH, high temperature, high ionic strength, and organic solvent conditions. Structure-activity relationship analysis indicates that sulfur atomic vacancy sites on MoS2 nanosheets are responsible for their catalytic activity. Furthermore, the lipoxygenase-like activity of MoS2 nanosheets was demonstrated within mammalian cells and animal tissues, inducing distinctive ferroptotic cell death. In summary, this research introduces an alternative to lipoxygenase to regulate lipid peroxidation in cells, offering a promising avenue for ferroptosis induction.

Pore-Scale Visualized Transport and Retention of Fibrous and Fragmental Microplastics in Porous Media under Various Surfactant Conditions.

For advancing current knowledge on the transport of microplastics (MPs) in the environment, this study used a real-time pore-scale visualization and quantitative system to examine the motions and mobility of fibrous and fragmental MPs under various surfactant (AEO, CTAC, and AES) and electrolyte conditions. The videos showed that fibrous MPs formed tangles through entanglement, which moved in an axial direction aligned with the flow streamline. Both fibrous and fragmental MPs showed suspended movement as well as surface movement (e.g., sliding, rolling, and saltating) in the porous media. Some deposited fibrous MPs showed flexible deformation due to shear flow. Compared to fragmental MPs, fibrous MPs showed lower mobility due to the tendency to deposit and clog the porous media. The mobility of fragmental MPs was enhanced in the presence of AEO but remained relatively unchanged with AES. In the presence of CTAC, the mobility of fragmental MPs was slightly inhibited under low ionic strength (IS) conditions but remarkably enhanced under high IS conditions. However, the mobility of fibrous MPs was largely unaffected by the surfactants. Both the numerical model and FDLVO calculations effectively described the transport and deposition of MPs in porous media.

Molecular dynamics simulations unveil the aggregation patterns and salting out of polyarginines at zwitterionic POPC bilayers in solutions of various ionic strengths

This study employs molecular dynamics (MD) simulations to investigate the adsorption and aggregation behavior of simple polyarginine cell-penetrating peptides (CPPs), specifically modeled as R9 peptides, at zwitterionic phosphocholine POPC membranes under varying ionic strengths of two peptide concentrations and two concentrations of NaCl and CaCl2. The results reveal an intriguing phenomenon of R9 aggregation at the membrane, which is dependent on the ionic strength, indicating a salting-out effect. As the peptide concentration and ionic strength increase, peptide aggregation also increases, with aggregate lifetimes and sizes showing a corresponding rise, accompanied by the total decrease of adsorbed peptides at the membrane surface. Notably, in high ionic strength environments, large R9 aggregates, such as octamers, are also observed occasionally. The salting-out, typically uncommon for short positively charged peptides, is attributed to the unique properties of arginine amino acid, specifically by its side chain containing amphiphilic guanidinium (Gdm+) ion which makes both intermolecular hydrophobic like-charge Gdm+ – Gdm+ and salt-bridge Gdm+ – C-terminus interactions, where the former are increased with the ionic strength, and the latter decreased due to electrostatic screening. The aggregation behavior of R9 peptides at membranes can also be linked to their CPP translocation properties, suggesting that aggregation may aid in translocation across cellular membranes.

Performance of delaying release and reducing adsorption of polyethyleneimine/poly(vinyl sulfonate) polyelectrolyte complex nanoparticles in polyacrylamide/polyethyleneimine gel system

Polyacrylamide/Polyethyleneimine (HPAM/PEI) is an environmentally friendly and promising gel system. However, inadequate gelation time and retention of the cross-linker (polyethyleneimine, PEI) during migration pose significant challenges for effective water control treatment in deep reservoirs. Polyelectrolyte complex nanoparticles (PECs) have demonstrated the ability to efficiently encapsulate PEI, facilitating for its gradual release. To achieve this, a cost-effective polyanionic complex, poly(vinyl sulfonate) (PVS), was employed to form PECs with PEI. By adjusting the mixing ratio of PEI and PVS, stable PECs suspensions with varying charges were successfully produced. These stable PECs exhibited spherical shapes with a particle size distribution ranging from 127.3–442.71 nm, and an average particle size of approximately 200 nm. The encapsulation efficiency of PEI by PECs varied from 64.56 % to 86.14 %. Under different conditions, 55.12 % to 90.26 % of PEI could be released from PECs. Increased temperatures, higher ionic strengths, and greater deviations in pH from the initial state of the PECs suspension all facilitated the release of PEI. The most stable PECs delayed the gelation time of the HPAM/PEI system to 9.5 days, which is twice the base gelation time of 4.5 days. The strength of mature HPAM/PEI (PECs) gels increased by 8.95 Pa in storage modulus (G′) compared to HPAM/PEI at the same concentration, albeit with a reduced linear viscoelastic region. And, the PECs-based delayed crosslinking method does not negatively affect the mechanical strength of the HPAM/PEI gel system, and thus its water control ability, under reservoir conditions. On the other hand, the static adsorption of PEI encapsulated by anionic PECs on sand decreased to one-fourth of that of free PEI (PEI solution). Additionally, the breakthrough of PEI encapsulated in anionic PECs in fractured sandstone cores was significantly advanced compared to free PEI.

Adsorption and Immobilization of Cadmium by an Iron-Coated Montmorillonite Composite

In this study, an iron-coated montmorillonite composite (FMC) was prepared, and the adsorption and immobilization of cadmium (Cd) was investigated. The composite was coated with spherical amorphous iron (Fe), which can promote the adsorption of Cd. At the fifth minute of adsorption, the rate of Cd adsorption by the FMC reached 97.8%. With temperature, the adsorption of Cd by FMCs first increases and then decreases. High pH can promote Cd adsorption; under the same ionic strength, the adsorption of Cd was greater by montmorillonite (Mont) than that by the FMC at pH < 4, but greater by FMC than that by Mont at pH > 4. High ionic strength had negative effects on Cd(II) adsorption by FMC and Mont, and ionic strength had less of an influence on the FMC than on Mont. Soil microorganisms promoted the dissolution of Fe and the release of Cd in the FMC. High temperature can promote the dissolution of Fe, but its effect on Cd release is not significant. At 32 °C, the Fe dissolution can promote Cd release in the FMC. Both the FMC and Mont reduced the bioavailability and leaching toxicity of Cd, reduced the exchangeable Cd, and increased the Fe-Mn bound and residual Cd. Overall, the FMC was more effective than Mont at immobilizing Cd.

Potential advantage of invasive estuarine worms over native species under exposure to relevant concentrations of graphene oxide: Behavioral and biochemical insights

Technological development using graphene oxide (GO) has increased in the last years, leading to the release of this contaminant to final sinks, such as estuaries. Due to their potential to flocculate and deposit when interacting with high ionic strength media, GO poses a threat, especially to benthic organisms like polychaetes. In addition to chemical contamination, estuaries also face a severe threat from invasive species, which can cause irreversible damage to ecosystems. The combination of abiotic and biotic stressors may work together on native species, decreasing their resilience. Thus, this study aims to assess the effects of an abiotic stressor, GO nanosheets (0.001, 0.01, 0.1, 1, 10 mg GO/Kg dw) on Hediste diversicolor (native species) and Arenicola marina (invasive species) through several behavioral assays and biochemical markers. The impact of invasive species A. marina (biotic factor) on H. diversicolor avoidance behavior was also evaluated. Obtained results demonstrated that H. diversicolor fled from lower GO contamination compartments to higher ones and that exposure to increased GO concentrations negatively impacted its burrowing activity. They were unable to escape from higher contamination compartments, but at the highest concentrations, the bioturbation activity was significantly higher, which may indicate that H. diversicolor tended to dwell deeper in the sediment. A. marina showed an escape behavior from compartments with higher GO concentrations. Additionally, this species' bioturbation activity significantly decreased when exposed to GO. Moreover, avoidance tests demonstrated that the presence of A. marina affected the behavior of H. diversicolor. Regarding oxidative stress, H. diversicolor seems to be more impacted than A. marina, since Lipid peroxidation levels were higher in all GO concentrations and Superoxide dismutase activity significantly increased in the lowest GO levels. Overall, H. diversicolor spatial distribution may be severely constrained under abiotic and biotic stress, while A. marina's higher foraging activity may promote its propagation in the estuary. Behavioral tests, combined with biochemical markers have shown to be relevant tools for the development of more environmental-realistic assessment and monitoring frameworks for estuaries.

Zika Virus NS1 Protein Detection Using Gold Nanoparticle-Assisted Dynamic Light Scattering.

The Zika virus (ZIKV) is a global health threat due to its rapid spread and severe health implications, including congenital abnormalities and neurological complications. Differentiating ZIKV from other arboviruses such as dengue virus (DENV) is crucial for effective diagnosis and treatment. This study presents the development of a biosensor for detecting the ZIKV non-structural protein 1 (NS1) using gold nanoparticles (AuNPs) functionalized with monoclonal antibodies employing dynamic light scattering (DLS). The biosensor named ZINS1-mAb-AuNP exhibited specific binding to the ZIKV NS1 protein, demonstrating high colloidal stability indicated by a hydrodynamic diameter (DH) of 140 nm, detectable via DLS. In the absence of the protein, the high ionic strength medium caused particle aggregation. This detection method showed good sensitivity and specificity, with a limit of detection (LOD) of 0.96 μg mL-1, and avoided cross-reactivity with DENV2 NS1 and SARS-CoV-2 spike proteins. The ZINS1-mAb-AuNP biosensor represents a promising tool for the early and accurate detection of ZIKV, facilitating diagnostic and treatment capabilities for arboviral infections.

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.

Insights into the Structural, Thermal/Dilatometric, and Optical Properties of Dy3+-Doped Phosphate Glasses for Lighting Applications.

Dysprosium-doped glasses are of interest for applications in light-emitting devices, yet the full range of effects of Dy3+ ions on glass properties is not fully understood. In this work, phosphate glasses with 50P2O5-(50 - x)BaO-xDy2O3 (0 ≤ x ≤ 4.0 mol %) nominal compositions were prepared by melting and the impact of Dy3+ ions on glass physical, structural, thermo-mechanical, and optical properties was evaluated. Following refractive index, density, and X-ray diffraction characterizations, the glasses were studied comprehensively through Raman spectroscopy, X-ray photoelectron spectroscopy, dilatometry, optical absorption, and photoluminescence (PL) spectroscopy. The thorough investigation and data analyses shed light on the Dy3+-driven structural and thermal properties reported here for the first time. The thermal expansion behavior was put in context with the reported data for other lanthanides and analyzed in the framework of the high ionic field strengths, leading to tighter glass networks. Further, a detailed analysis of the absorption, PL, and emission decay curves was carried out, providing insights into the origin of the optical behavior. Supported is the hypothesis that the cross-relaxation channels between Dy3+ ions taking place at low concentrations are responsible for the decrease in the decay times while the PL attractive for lighting applications still improves. Conversely, high Dy3+ concentrations facilitate the emission quenching proceeding via an electric dipole-dipole interaction likely incorporating the resonant excitation migration pathway for Dy3+-Dy3+ mean distances shorter than ∼15 Å.

Dual cation Kgu/PAM Gel polymer electrolyte with high ionic conductivity and mechanical strength for flexible All-Solid-State supercapacitors

Gel polymer electrolytes (GPEs) have attracted much attention due to their excellent flexibility, good interface contact, and high safety in solid-state supercapacitors (SSCs). However, in practical applications, GPEs still face low ionic conductivity and poor mechanical strength. This study delineates a novel dual-cationic Kgu/PAM GPE, the ion diffusion coefficients in which are 1.51 × 10-8 cm2 s−1 (K+) and 4.77 × 10-9 cm2 s−1 (Na+), respectively. Radial distribution function and in-situ Fourier transform infrared spectroscopy have confirmed that the migration mechanism of dual-cations in Kgu/PAM is through the long-range hydration channels, which is depended on the continuous formation of binding water facilitated by movement of Kgu and PAM chain segments. When assembled dual-cationic Kgu/PAM GPE to a flexible solid-state asymmetric supercapacitor, it delivers a high ionic conductivity (86.9 mS cm−1), an excellent energy rate density (86.1 Wh kg−1) and outstanding power density (476 W kg−1). In addition, dual-cationic Kgu/PAM GPE exhibits an excellent strain threshold of 910 % and remarkable mechanical strength of 35 KPa, good flexibility and flame retardant, highlighting the potential for its practical application in various fields. Collectively, these findings herald a novel paradigm in the development of secure and efficacious flexible wearables.

Evaluation of extraction and storage conditions for quantification and characterization of silver nanoparticles in complex samples by single particle-ICP-MS

The extraction of nanoparticles (NPs) from complex matrices and subsequent storage can potentially alter the NPs physicochemical properties and hinder cross-study comparisons. Most NPs extraction methods are designed and tested at high NPs concentrations, although (eco)toxicological and regulatory monitoring programs require methods capable of analyzing NPs at environmentally relevant concentrations (lower ppb range). In this study, we investigated how extraction methods affect the characteristics of PVP coated and citrate-stabilized silver NPs (AgNPs) spiked into soil, sewage sludge, and biological samples at environmentally relevant concentrations using Single Particle Inductively Coupled Plasma Mass Spectrometry spICP-MS). Further we investigated the impact of storage temperature (-80 °C – 21 °C) and storage duration (1–28 days) on the particle characteristics such as particle size.We found that aqueous AgNPs samples with low ionic strength media retained their original characteristics (like particle size, particle concentration and particle-based Ag mass) when preserved at 4 °C for up to 28 days. AgNPs dispersed in high ionic strength media were however better preserved at −80 °C. Among the extraction agents, tetrasodium pyrophosphate was efficient in extracting AgNPs from soil and sewage sludge matrices, while Proteinase K was most suitable for biological samples from organisms (earthworms or fish).Although our study focused only on AgNPs, it provides crucial information to aid interlaboratory comparisons and data interpretation for (eco)toxicological studies.

Dual-mode immunochromatography based on Ti3C2Tx functionalized CdTe quantum dots for chloramphenicol detection in animal-derived foods

In this study, Ti3C2Tx was coupled with CdTe quantum dots via plyethylenimine (PEI) mediation to form composite nanomaterials with dual colorimetric and fluorescent properties, which had strong pH, high ion strength, and organic solvent resistance. Then, this novel Ti3C2Tx@CdTe was firstly applied to develop a dual-mode immunochromatographic assay (ICA) for chloramphenicol (CAP) detection in animal-derived foods. The limits of detection of the colorimetric and fluorescent modes for CAP in milk/chicken/fish were 0.01 and 0.005 μg/kg, the limits of quantification were 0.025 and 0.016 μg/kg, the recovery rates were between 85.7% and 129.0% and 84.0%-119.2%, with the corresponding variations ranged from 6.5% to 14.8% and 6.4%-14.9%, respectively. The sensitivity of fluorescence mode was up to 100-fold higher than that of the reported ICA for CAP detection. The results of the confirmatory experiment on 30 samples showed good consistency with that of our established method (R2>0.93). The above results indicated that Ti3C2Tx@CdTe had superior detection performance and can provide a dual-mode signal calibration, high stability and sensitivity selection for immunoassay detection platforms.

Removal of sulfamethoxazole using Fe-Mn biochar filtration columns: Influence of co-existing polystyrene microplastics

Emerging contaminants, particularly antibiotics and microplastics (MPs), present significant challenges in wastewater treatment and pose large ecological risks. This study investigates the removal efficiency of sulfamethoxazole (SMX) using Fe-Mn modified biochar (BFM) in fixed bed filtration columns, emphasizing the effect of the presence of polystyrene microplastics (PS-MPs) on SMX behavior in both water (pH ≈ 5.6) and selected wastewater (pH ≈ 8) systems. Batch sorption results show that 10 mg/L SMX in 50 mL water can be completely removed by 100 mg BFM sorbent. The Bed Depth Service Time model indicated the BFM column is feasible for SMX removal in scaled-up continuous wastewater flow operations, while the Yan model best elucidates SMX filtration behavior and suggests the dominant adsorption mechanisms include external mass transfer and intraparticle diffusion. The present of both 20 mg/L and 100 mg/L PS-MPs (pH ≈ 5.6) significantly reduced SMX retention due to competitive sorption. However, at pH 3.2, competitive sorption became negligible due to electrostatic interactions driving the PS-MPs sorption, while neutral charged SMX bound through hydrogen-bonds or π-π EDA interactions. Elevated pH shifted both PS-MPs and SMX sorption to non-electrostatic thus intensifying sorption competition, highlighting the influence of pH on their interaction dynamics. In wastewater, SMX filtration was slightly inhibited by 100 mg/L PS-MPs in BFM columns, whereas PS-MPs removal remained unaffected due to the high ionic strength and alkaline pH. These findings highlight the impact of MPs on pollution removal efficiency in filtration system, essential for enhancing biochar-based wastewater treatment strategies.

Nanobubble-enabled foam fractionation to remove algogenic odorous micropollutants

Due to climate change and environmental pollution, natural lakes and reservoir water suffer increasingly serious algal blooms and associated water quality problems due to the presence of algal or algogenic organic matter (AOM) such as algal odour and toxins. Effective removal of these micropollutants, especially in the event of algal blooms, is critical to aesthetic values of water bodies, drinking water security and human health. The study investigated the removal efficiency of two common odorous compounds, trans-1,10-dimethyl-trans-9-decalol (geosmin) and 2-Methylisoborneol (2-MIB), using foam fractionation enabled by air nanobubbles with addition of two common cationic and anionic surfactants, sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB), to enhance foaming ability and stability. The results showed that the cationic surfactant (i.e., CTAB), a low pH, and high ionic strength significantly promoted the removal of geosmin and 2-MIB. For example, the removal tests using the synthetic water determined that the conditions of pH = 7, [CTAB] = 20 mg·L−1 and IS = 10 mM as NaCl resulted in both the highest geosmin removal rate of 91.81% and highest 2-MIB removal rate of 85.0%. The removal of two odorous compounds in real lake water was evaluated, which yielded removal rates of 83.2% for geosmin and 48.1% for 2-MIB, highlighting the minor inhibition from water matrixes on the removal performances. Compared to microbubbles, nanobubbles enabled greater surface areas of foam and higher removal efficiencies. The study provided new insights into the use of foam fractionation with air nanobubbles to enhance the removal of odorous compounds from impaired water and mitigate the negative environmental and health impacts of harmful algal blooms (HABs).

Halocins and C50 Carotenoids from Haloarchaea: Potential Natural Tools against Cancer.

Haloarchaea are a group of moderate and extreme halophilic microorganisms, belonging to the Archaea domain, that constitute relevant microbial communities in salty environments like coastal and inland salted ponds, marshes, salty lagoons, etc. They can survive in stress conditions such as high salinity and, therefore, high ionic strength, high doses of ultraviolet radiation (UV), high temperature, and extreme pH values. Consequently, most of the species can be considered polyextremophiles owing to their ability to respond to the multiple extreme conditions characterizing their natural habitats. They cope with those stresses thanks to several molecular and metabolic adaptations. Thus, some of the molecules produced by haloarchaea show significantly different biological activities and physicochemical properties compared to their bacterial counterparts. Recent studies have revealed promising applications in biotechnology and medicine for these biomolecules. Among haloarchaeal biomolecules, rare natural pigments (C50 carotenoids) and small peptides called halocins and microhalocins have attracted attention worldwide due to their effects on animal and human commercial tumoral cells, apart from the role as antibiotics described for halocins or the immunomodulatory activity reported from C50 carotenoids like bacterioruberin. This review summarizes recent knowledge on these two types of biomolecules in connection with cancer to shed new light on the design of drugs and new therapies based on natural compounds.