Strong Ion Research Articles

Oral but Not Topical Sodium Bicarbonate Improves Repeated Sprint Performance During Simulated Soccer Match Play Exercise in Collegiate Athletes.

This study investigated the effect of oral and topical sodium bicarbonate (SB) on soccer-specific performance during simulated soccer exercise. In a block randomized, double-blind, crossover design, 10 collegiate male soccer players (stature: 181.7 ± 3.2cm, body mass: 81.7 ± 10.5kg) performed soccer-specific performance tests (countermovement jumps, Illinois agility, 8 × 25m repeated sprints) throughout a 90-min soccer-specific aerobic field test (SAFT90) following 0.3g/kg body mass SB in capsules (SB-ORAL), 0.9036g/kg body mass PR Lotion (SB-LOTION), or placebo capsules and lotion (PLA). Soccer-specific performance tests were conducted pre-SAFT90, during half-time and post-SAFT90. Blood samples were analyzed for acid-base balance (pH; bicarbonate, HCO3-) and strong ions (sodium, Na+; potassium, K+). Average sprint times were quicker for SB-ORAL than PLA during half-time (3.7%; p = .049; g = .57) and post-SAFT90 (4.9%; p = .041; g = .66). SB-ORAL increased pH and HCO3- prewarm-up and during half-time (p < .05), and lowered K+ during half-time (p = .035) compared with PLA. SB-LOTION increased pH (p = .019) and lowered K+ (p = .012) during half-time compared with PLA. SB-LOTION increased Na+ postexercise compared with PLA (p = .008). Repeated sprint times during simulated soccer exercise improved for SB-ORAL, which might have been mechanistically underpinned by elevated blood buffering capacity and greater regulation of strong ion concentration. Consuming SB in capsules is a more effective strategy than topical SB application for improving blood buffering capacity and repeated sprint performance throughout competitive soccer matches.

&amp;nbsp;Synthesis and Characterization of Chitosan-Based Schiff Base and Cu(II) Complex from Shrimp Shells and its Application on Catalysis and Bio-sorption

In recent years, metal complexes and biopolymers have gained significant attention in environmental applications such as catalysis and heavy metal removal. Chitosan, a biopolymer derived from chitin, is well-known for its biodegradability, non-toxicity, and strong metal ion affinity, which can be further enhanced through Schiff bases to improve its catalytic and adsorption capabilities. The primary objectives of this study were to investigate whether Cu(II) complex of Chitosan Salicylaldehyde Schiff Base CSSB-Cu(II) can act as an efficient catalyst in hydrogen peroxide decomposition reaction and to find out the raw absorbent which has the highest Cadmium ion removal efficiency from among the absorbents Chitin (CT), Chitosan (CS) and Chitosan Salicylaldehyde Schiff Base (CSSB). CSSB was synthesized using the Schiff condensation reaction between the amino group of CS and the carbonyl compound of salicylaldehyde with the elimination of water molecules and it was complexed with Cu(II) ion to produce CSSB-Cu(II) complex. The catalytic effect of the CSSB-Cu(II) complex on the kinetics of the decomposition of hydrogen peroxide was investigated and compared with CSSB. CSSB-Cu(II) showed a better catalytic effect than CSSB and has a pseudo-first-order catalytic decomposition for H2 O2 . CT, CS, and CSSB were investigated as adsorbents for the Cd(II) removal to determine their cadmium removal efficiencies. This study concludes that the removal efficiency of CSSB was greater than that of CS and CT. The equilibrium data agreed more with the Langmuir model than with the Freundlich model. The IR and electronic spectral data confirm the presence of an imine bond and the existence of the complex in square planar geometry.

Ponderomotive potential effects on strong field two-photon double ionization in neon

Abstract In the context of the recently reported experiment on photoionization in neon atom, we theoretically study the photoionization of neon atom at a comparatively intense laser field. The calculated photoelectron spectrum for a Gaussian laser pulse show an asymmetric double peak line shape at a pulse duration of 14.2 fs and peak intensity of 1x1015 W/cm2. A systematic study clearly indicates that the ponderomotive potential of the photoelectron released during photoionization of neon is instrumental in causing the visible asymmetry. &amp;#xD; Interestingly, for similar laser parameters asymmetry in the the photoelectron spectrum gets significantly reduced for a Sech2&amp;#xD;shaped laser pulse. Time resolved photoelectron spectrum reveals that even for a Sech2 shaped laser pulse the two peak photoelectron spectrum is initially asymmetric and evolves into a symmetric line shape with increase in time. The results clearly indicate that irrespective of laser pulse shape asymmetry shows a non-linear decrease as a function of time. Our study also shows the possibility of controlling the asymmetry by varying the pulse duration. The calculations establishes a correlation between the effects of direct double ionization and ponderomotive potential on the asymmetry of the photoelectron spectrum at different pulse durations.&amp;#xD;

Heat-Resistant Covalent Organic Framework (COF) PVA-Hybridized Gel Electrolyte for the Preparation of Dendrite-Free Zinc-Ion Batteries.

High-performance zinc-ion batteries (ZIBs) have attracted a great deal of attention due to their high theoretical capacity and high level of safety. Herein, we propose a covalent organic framework (COF) hybrid poly(vinyl alcohol) (PVA)-based gel electrolyte, which can induce the uniform deposition of Zn2+ and achieve dendrite-free formation. By grafting sulfonic acid groups on the surface of COFs to absorb Zn2+, we can strengthen the interaction between strong ions and dipoles in the electrolyte, improve the ionic conductivity, and achieve stable Zn2+ electroplating and stripping. Due to the good thermal stability of the COF material itself, the gel electrolyte hybrid with the PVA hydrogel shows high mechanical strength and good heat resistance and is capable of stable cycling for >1000 h at 50 °C, with a capacity retention rate of ≤75%. This study provides a new approach for developing high-temperature-resistant and highly stable dendrite-free ZIBs.

Chemical Composition and Biological Activity of Hypericum Species-H. hirsutum, H. barbatum, H. rochelii.

St. John's wort (Hypericum perforatum, Hypericaceae) is the most well-known species in the genus Hypericum, which comprises several hundred species. This study investigates the biological and phytochemical potential of the under-researched Hypericum species, H. hirsutum, H. barbatum, and H. rochelii. A high level of similarity between the chemical profiles of H. hirsutum and H. barbatum and the official source of the herbal drug (H. perforatum) was shown, but a higher content of quercetin and rutin was also found in all three evaluated species (116-230 µg/g dry herb). The highest amount of phenolics (195 mg GAE/g) was recorded in H. hirsutum extract, while the highest amount of flavonoids (47 mg QE/g) was recorded in H. barbatum extract. The evaluated species were excellent scavengers of DPPH, OH, and NO radicals, as well as strong ferric ion reducers in the FRAP test. Prominent monoamine oxidase A and α-glucosidase inhibition was observed, compared to modest inhibition of monoamine oxidase B, α-amylase, and acetylcholinesterase. High activity against Gram-positive MRSA S. aureus was demonstrated for the tested species, with MIC/MBC values recorded at 12.5 µg/mL. Antifungal activity against Candida strains was not observed. The obtained results emphasize the need for further investigation of species of the genus Hypericum to discover potentially new sources of biologically active compounds.

Electrochemical Selective Removal of Oxyanions in a Ferrocene-Doped Metal-Organic Framework.

Metal-organic frameworks (MOF) are a class of crystalline, porous materials possessing well-defined channels that have widespread applications across the sustainable landscape. Analogous to zeolites, these materials are well-suited for adsorption processes targeting environmental contaminants. Herein, a zirconium MOF, UiO-66, was functionalized with ferrocene for the selective removal of oxyanion contaminants, specifically NO3-, SO42-, and PO43-. Electrochemical oxidation of the embedded ferrocene pendants induces preferential adsorption of these oxyanions, even in the presence of Cl- in a 10-fold excess. Anion selectivity strongly favoring PO43- (Soxy/comp = 3.80) was observed following an adsorption trend of PO43- > SO42- > NO3- > (10-fold)Cl- in multi-ion solution mixtures. The underlying mechanisms responsible for ion selectivity were elucidated by performing ex situ X-ray photoelectron spectroscopy (XPS) on the heterogeneous electrode surface postadsorption and by calculating the electronic structure of various adsorption configurations. It was eventually shown that oxyanion selectivity stemmed from strong ion association with a positively charged pore interior due to the spatial distribution of charge by oxygen constituents. While ferrocenium provided the impetus for ion migration-diffusion, it was the formation of stable complexes with zirconium nodes that ultimately contributed to selective adsorption of oxyanions.

Enhanced Removal of Chlorpyrifos, Cu(II), Pb(II), and Iodine from Aqueous Solutions Using Ficus Nitida and Date Palm Biochars

This study explores the adsorption efficiency of biochar derived from palm trees and Ficus nitida for the removal of various contaminants, including Cu(II), Pb(II), iodine, and chlorpyrifos from aqueous solutions. Biochar was prepared using a two-step pyrolysis process for date palm biochar and single-step pyrolysis for Ficus nitida biochar. Characterization techniques such as SEM, EDX, and FTIR revealed a significant surface area and a variety of functional groups in both types of biochar, essential for effective adsorption. The date palm biochar exhibited superior adsorption capacities for Cu(II) and Pb(II) ions, achieving efficiencies up to 99.9% and 100%, respectively, due to its high content of oxygen-containing functional groups that facilitated strong complexation and ion exchange mechanisms. Conversely, Ficus nitida biochar demonstrated a higher adsorption capacity for iodine, reaching 68% adsorption compared to 39.7% for date palm biochar, owing to its greater surface area and microporosity. In the case of chlorpyrifos, Ficus nitida biochar again outperformed date palm biochar, achieving a maximum adsorption efficiency of 87% after 24 h of incubation, compared to 50.8% for date palm biochar. The study also examines the effect of incubation time on adsorption efficiency, showing that the adsorption of chlorpyrifos by date palm biochar increased significantly with time, reaching a maximum of 62.9% after 48 h, with no further improvement beyond 12 h. These results highlight the importance of biochar characteristics, such as surface area, pore structure, and functional groups, in determining adsorption efficiency. The findings suggest that optimizing pyrolysis conditions and surface modifications could further enhance the performance of biochar as a cost-effective and sustainable solution for water purification and environmental remediation.

An algorithmic approach to arterial blood gas analysis for cardiologists

Abstract: An arterial blood gas (ABG) is a laboratory test to monitor the patient’s acid base balance. The body regulates pH closely to maintain homeostasis. This test is used to determine the magnitude of the compensation by the buffer system and includes the measurements of the acidity (pH), levels of oxygen, and carbon dioxide in arterial blood. Acid base disorders can lead to severe complications in many disease states. ABG interpretation is paramount in critically ill patients. Many methods already exist to guide the interpretation of the ABG. This article does not include methods such as analysis of base excess or Stewart’s strong ion difference. It is paramount for cardiologists to understand ABG interpretation to manage their patients effectively. Interpreting ABGs may seem complex, but a systematic approach is required to diagnose and treat disorders by quick and easy ABG interpretation.

Synergistic enhancement of g-C3N4/CoAl-LDH nanoflower and mineral admixtures on the properties of nano-engineered cementitious composites

The nano-engineered cementitious composites (NCC) were prepared using g-C3N4/CoAl-LDH nanoflower (nano-CN/L), in combination with mineral admixtures including fly ash (FA), metakaolin (MK), and ground granulated blast furnace slag (GGBFS). The synergistic effects and mechanisms of nano-CN/L and mineral admixtures on the mechanical, chloride penetration resistance and air purification properties of NCC were investigated. The results show that nano-CN/L promotes the early hydration of cementitious materials and improves the composition and morphology of C-S-H gel. Furthermore, the filling effect of nano-CN/L significantly optimizes the pore structure and interfacial crack width of NCC, thereby eliminating the adverse impact of FA, MK, and GGBFS on its early mechanical strengths. Additionally, nano-CN/L enhances the chloride penetration resistance and NOx removal properties of NCC through its strong ion adsorption and photocatalytic activity, respectively. Incorporating 0.9 % nano-CN/L by mass of cementitious materials reduces the chloride diffusion coefficient of NCC at curing age of 56d by 26.9 % and increases the NOx removal ratio by 11 times. The 7d’s compressive and flexural strengths of NCC increase by 13.6 % and 4.6 %, respectively, compared to the one without nano-CN/L. As a novel multifunctional nanomaterial, nano-CN/L not only provides a new pathway for extending the service life of cementitious composites, but also injects new momentum into their environmental-friendly development.

Spontaneous asymmetry effect induced by uniform magnetic fields in capacitively coupled plasmas under perfectly symmetric conditions

Abstract Introducing asymmetry in capacitively coupled plasmas (CCPs) is a common strategy for achieving independent control of ion mean energy and flux. Our 1d3v particle-in-cell/Monte Carlo collision simulations reveal that a uniform magnetic field within a specific range can induce spatial asymmetry in low-pressure CCPs, even under perfectly symmetric conditions. This asymmetry, characterized by a shift in the plasma density distribution and significant differences in electron kinetics between the two sides of the plasma, leads to strong ionization and most electron losses on the low-density side, while the high-density side experiences weak ionization and minimal electron losses. The underlying mechanism triggering this spontaneous asymmetry is the differential influence of the magnetic field on low-energy (local) and high-energy (relatively nonlocal) electrons. Under conditions of low pressure and an appropriate magnetic field, this disparity in electron kinetic behavior leads to a spontaneous amplification of the asymmetry induced by random fluctuations until a steady state is reached, culminating in a spontaneous asymmetric effect.

Comparison between the dilution of electrolyte concentrate in milk or water for oral rehydration of diarrheal calves

The administration of oral electrolyte solution (OES) is the most used method to correct dehydration and electrolyte and acid-base imbalances in calves with diarrhea. To prepare OES, the electrolyte concentrate (EC) is diluted in water. Alternatively, it can be diluted in milk and the correction of dehydration depends on voluntary water intake. Although dilution in milk is used, its efficacy has not been fully proven. This study compared the effectiveness of two rehydration methods in correcting imbalances in diarrheal calves. Twenty-four neonatal calves with induced osmotic diarrhea were distributed into two treatment groups using a commercial EC: GM with EC diluted in the milk at meals; and GW with EC diluted in water (volumes of 5% BW, at 4 and 12 h). All were fed with milk (volumes of 4% BW, at 0, 8, and 16 h) and had free access to water. Clinical and laboratory variables were monitored over time up to 48 h. The calves presented moderate dehydration, hyponatremia, relative hyperchloremia and moderate strong ion metabolic acidosis. Both rehydration methods were effective in correcting imbalances and reestablishing plasma SID3 at the end of the day of treatment. Plasma volume expansion was faster in GW. Electrolyte-enriched milk is as efficient as OES for treating diarrheal calves.

Polyethyleneimine Modified Two-Dimensional GO/MXene Composite Membranes with Enhanced Mg2+/Li+ Separation Performance for Salt Lake Brine.

As global demand for renewable energy and electric vehicles increases, the need for lithium has surged significantly. Extracting lithium from salt lake brine has become a cutting-edge technology in lithium resource production. In this study, two-dimensional (2D) GO/MXene composite membranes were fabricated using pressure-assisted filtration with a polyethyleneimine (PEI) coating, resulting in positively charged PEI-GO/MXene membranes. These innovative membranes, taking advantage of the synergistic effects of interlayer channel sieving and the Donnan effect, demonstrated excellent performance in Mg2+/Li+ separation with a mass ratio of 20 (Mg2+ rejection = 85.3%, Li+ rejection = 16.7%, SLi,Mg = 5.7) in simulated saline lake brine. Testing on actual salt lake brine in Tibet, China, confirmed the composite membrane's potential for effective Mg2+/Li+ separation. In the actual brine test with high concentration, Mg2+/Li+ after membrane separation is 2.2, which indicates that the membrane can significantly reduce the concentration of Mg2+ in the brine. Additionally, the PEI-GO/MXene composite membrane demonstrated strong anti-swelling properties and effective divalent ion rejection. This research presents an innovative approach to advance the development of 2D membranes for the selective removal of Mg2+ and Li+ from salt lake brine.

Urinary chloride excretion in critical illness and acute kidney injury: a paediatric hypothesis-generating cohort study post cardiopulmonary bypass surgery.

Renal chloride metabolism is currently poorly understood but may serve as both a diagnostic and a treatment approach for acute kidney injury. We investigated whether plasma chloride, ammonia and glutamine as well as urinary chloride, ammonium and glutamine concentrations may serve as markers for acute kidney injury in paediatric patients. We conducted a prospective observational trial in a tertiary care paediatric intensive care unit. Ninety-one patients after cardiopulmonary bypass surgery were enrolled. Plasma glutamine, creatinine, (serum) albumin, urinary electrolytes and glutamine were collected pre-cardiopulmonary bypass surgery, at paediatric intensive care unit admission, and at 6, 12, 24, 48 and 72 h after paediatric intensive care unit admission. The urinary strong ion difference was calculated. The median urinary chloride excretion decreased from 51 mmol/L pre-cardiopulmonary bypass to 25 mmol/L at paediatric intensive care unit admission, and increased from 24 h onwards. Patients with acute kidney injury had lower urinary chloride excretion than those without. The median urinary strong ion difference was 59 mmol/L pre-cardiopulmonary bypass, rose to 131 mmol/L at 24 h and fell to 20 mmol/L at 72 h. The plasma chloride rose from 105 mmol/L pre-cardiopulmonary bypass to a maximum of 109 mmol/L at 24 h. At 24 h the plasma chloride concentration was associated with the presence of acute kidney injury. There was no association between plasma or urinary amino acids and chloride excretion or kidney injury. In conclusion, renal chloride excretion decreased in all patients, although this decrease was more pronounced in patients with acute kidney injury. Our findings may reflect a response of the kidneys to critical illness, and acute kidney injury may make these changes more pronounced. Targeting chloride metabolism may offer treatment approaches to acute kidney injury.

The Role of Carrier Ion‐Ligand Interaction on Intercalation Potentials and Phase Evolution of Berlin Green Cathodes in Rechargeable Batteries

AbstractIntercalation and deintercalation are fundamental processes in battery electrodes that involve the reversible addition and extraction of carrier ions such as lithium (Li) and sodium (Na) into a host framework made of transition metal (TM) ions and ligands. Although TM–ligand interactions are known to primarily determine intercalation potentials, a comprehensive understanding of their interactions involving the carrier ions still remains elusive. This study investigates the complex interactions between carrier ions (Li and Na) and the ligand in Berlin green (BG, Fe3+[Fe3+(CN)6]) cathodes to elucidate their effects on intercalation potentials and phase evolution. Comprehensive X‐ray characterizations and electrochemical analyses reveal that the strong carrier ion–ligand interaction, influenced by the type and concentration of carrier ions, can modify the electronic structure of Fe ions and affect the intercalated structure of BG cathodes, thereby tuning the intercalation potentials. Specifically, the enhanced covalent interaction of the Na–CN units compared with that of the Li–CN units induces rhombohedral distortion in the fully sodiated state and increases the working potential of high‐spin Fe ions. The findings highlight the critical role of carrier ion–ligand interactions in tuning the electrochemical properties of battery electrodes for the design of advanced battery systems.

Specific ion effects on the soil shear strength and clay surface properties of collapsing wall in Benggang.

Benggangs are a special type of soil erosion in the hilly granite regions of the tropical and subtropical areas of Southern China. They cause severe soil and water loss, which can severely deteriorate soil quality and threat to the local ecological environment. Soils (red soil, sandy soil and detritus soil) were collected from collapsing wall of a typical Benggang in Changting County of Fujian Province, and their physicochemical and mineralogical properties were analyzed. Five different monovalent cations were used to saturate the soil samples to examine the specific ion effects on the shear strength and clay surface properties. Red soil had a higher clay content, plastic limit, liquid limit and shear strength than sandy soil and detritus soil. The studied soils mainly consisted of kaolinite, hydroxy-interlayer vermiculite, illite and gibbsite clay minerals. The soils saturated with K+, NH4 +and Cs+ had greater cohesion than the Li+- and Na+-saturated soils, e.g., the cohesion of the red soil saturated with Li+, K+, NH4 + and Cs+ cations were 1.05, 1.23, 1.45 and 1.20 times larger than that of the Na+-saturated soil, respectively. While the internal friction angle was slightly different, which indicated that different monovalent cations affected the shear strength differently. K+-, NH4 +- and Cs+-saturated clay particles had higher zeta potentials and thinner shear plane thicknesses than Li+- and Na+-saturated clay particles and showed strong specific ion effects on the clay surface properties. The changes in clay surface properties strongly affected the soil mechanical properties. Soils saturated with K+, NH4 + and Cs+ could increase the shear strength, and then increase the stability of the collapsing wall, thus might decrease the erosion intensity of Benggang. The results provide a scientific basis for the interpretation of and practical treatment of Benggang.

SERIAL CHANGES IN METABOLIC ACID-BASE STATUS IN THREE SPECIES OF ANESTHETIZED CAPTIVE LARGE FELID.

Determination of acid-base status contributes important information about patient health, including for patients under anesthesia. There is a paucity of information about the determinants of acid-base status of large felids managed under anesthesia, and advancement of such knowledge may contribute to patient safety. This study serially monitored the individual metabolic acid-base status of 11 large felids, including lions (Panthera leo), tigers (Panthera tigris), and cheetahs (Acinonyx jubatus), under general anesthesia. We analyzed the contributions of measured strong ions (sodium, chloride, potassium, lactate), weak acids and buffers (albumin, phosphate and bicarbonate), and unmeasured anions to standardized extracellular base excess (SBE). A general linear model assessed for species differences in these parameters, with time since immobilization, SBE, and mean arterial pressure as covariates. By employing a Stewart-based analytical approach, it was possible to separate chloremic and unmeasured anion contributions to metabolic acid base status. This provided a basis for identifying mixed metabolic processes, generating differentials for underlying causes. Using normal acid base parameters for domestic felids, metabolic acidosis was found to be prevalent. Frequent evidence of unmeasured anion accumulation was also found, with unmeasured anions occasionally exceeding 5mmol/L. These findings warrant further inquiry into the drivers and clinical significance of metabolic acidosis and unmeasured anion accumulations in anesthetized large felids, encouraging further anion identity studies to elucidate possible causes. Reference ranges need to be established for acid-base parameters in large felids as a foundation for interpreting more controlled, prospective research into determinants of metabolic acid-base status in these animals under anesthesia.

Acute renal response to changes in carbon dioxide in mechanically ventilated female pigs.

Kidney response to acute and mechanically induced variation in ventilation associated with different levels of PEEP has not been investigated. We aimed to quantify the effect of ventilatory settings on renal acid-base compensation. Forty-one pigs undergoing hypo- (<0.2 Lkg-1 min-1, PEEP 25 cmH2O), intermediate (0.2-0.4 Lkg-1 min-1 with either PEEP 5 or 25 cmH2O), or hyper-ventilation (>0.4 Lkg-1 min-1, PEEP 5 cmH2O) for 48 h were retrospectively included. The decrease in pH paralleled the decrease in plasma strong ion difference (SID) in hyper- and intermediately ventilated groups with lower PEEP. In contrast, the plasma SID remained nearly constant in hypo- and intermediately ventilated groups with higher PEEP. Changes in plasma chloride concentration accounted for the changes in plasma SID (conditional R2 = 0.86). The plasma SID changes were paralleled by mirror changes in urinary SID. Higher PEEP (25 cmH2O), compared to lower PEEP (5 cmH2O) dampened or abolished the renal compensation through its effect on hemodynamics (higher central venous and mean pulmonary pressures), irrespective of minute ventilation. During mechanical ventilation, the compensatory renal response to respiratory derangement is immediate and progressive but can be dampened by high PEEP levels.

Boosting the rate performance of zinc-iodine batteries via electrostatic adsorption and catalysis of strong base ion resin grafted with cobalt phthalocyanine

The shuttle of iodine species is considered the obstacle to the application of aqueous zinc iodine (Zn-I2) batteries. Although cathode hosts with electrostatic adsorption to iodine species have been developed to suppress the shuttle effect of polyiodide, the strong interaction between polyiodide and hosts significantly slow down the kinetics of oxidation–reduction of iodine species. Here, a host with strong constraint and catalytic effects on iodine species based on strong base ion exchange resin is established, while the interaction and catalytic performance of hosts on iodine species is regulated by adjusting the functional group structure and the loading amount of quaternary ammonium cobalt phthalocyanine (QACoPc). UV–vis spectroscopy and electrochemical characterization confirm that the iodine host suppresses the shuttle of polyiodide. Moreover, the kinetic analyses reveal that the introduction of QACoPc into host improves the redox kinetic process of iodine species. Consequently, the polymer-based Zn-I2 battery exhibits stable cycling ability (98.9 % retention rate after 2000 cycles at the current density of 10 C, 1 C: 160 mAh g−1) and excellent rate performance (150.6 mAh g−1 at 1 C and 105.9 mAh g−1 at 50 C) due to the strong constraint and catalytic effects of host on iodine species.

Structural Characterization and Biological Properties Analysis of Exopolysaccharides Produced by Weisella cibaria HDL-4.

An exopolysaccharide (EPS)-producing strain, identified as Weissella cibaria HDL-4, was isolated from litchi. After separation and purification, the structure and properties of HDL-4 EPS were characterized. The molecular weight of HDL-4 EPS was determined to be 1.9 × 10⁶ Da, with glucose as its monosaccharide component. Fourier transform infrared spectroscopy (FT-IR) and nuclear magnetic resonance (NMR) analyses indicated that HDL-4 EPS was a D-glucan with α-(1→6) and α-(1→4) glycosidic bonds. X-ray diffraction (XRD) analysis revealed that HDL-4 EPS was amorphous. Scanning electron microscope (SEM) and atomic force microscope (AFM) observations showed that HDL-4 EPS possesses pores, irregular protrusions, and a smooth layered structure. Additionally, HDL-4 EPS demonstrated significant thermal stability, remaining stable below 288 °C. It exhibited a strong metal ion adsorption activity, emulsification activity, antioxidant activity, and water-retaining property. Therefore, HDL-4 EPS can be extensively utilized in the food and pharmaceutical industries as an additive and prebiotic.

Ion Correlation-Driven Hysteretic Adhesion and Repulsion between Opposing Polyelectrolyte Brushes.

Polyelectrolyte (PE) brushes are widely used in biomaterials and nanotechnology to regulate the surface properties and interactions. Here, we apply the electrostatic correlation augmented self-consistent field theory to investigate the interactions between opposing PE brushes in a mixture of 1:1 and 3:1 salt solutions. Our theory predicts a hysteretic feature of the normal stress induced by strong ion correlations. In the presence of trivalent ions, the force profile is discontinuous: repulsive in the compression branch and adhesive in the separation branch. The molecular origin of the hysteretic force is the coexistence of two collapsed modes: two separated condensed layers on each surface in the compression and a single bundled condensed layer in the separation. With the systematic inclusion of ion correlations, our theory captures well the hysteretic force, adhesive separation, "jump-in" and "jump-out" features, and the "specific ion effect", all in good agreement with the reported experimental results.