Stability Of Salts Research Articles

Polysaccharide-Based Coacervate Microgel Bearing Cationic Peptides That Achieve Dynamic Cell-Membrane Structure Alteration and Facile Cytosolic Infusion of IgGs.

Conjugates of the biocompatible polysaccharide pullulan with a cell membrane permeabilizing peptide L17E (PL-L17Es) were prepared with the aim of producing complex coacervates with pronounced intracellular antibody (IgG) delivery activity and stable structures. Coacervates with diameters of a few μm were formed simply by mixing PL-L17Es with IgG labeled with negatively charged fluorescent moieties of Alexa Fluor 488 [IgG(AF488)]. The coacervate resulted in a pronounced cytosolic infusion of IgG(AF488) and IgG binding to the target proteins inside the cell. The droplet structures were maintained even under high salt conditions, and the fluorescence in the droplet was not recovered after photobleaching, suggesting the formation of complex coacervate microgels. Dynamic changes in cell membrane structure to entrap the coacervate microgels were captured by confocal and electron microscopy, resulting in cytosolic IgG infusion. The use of M-lycotoxin instead of L17E resulted in a coacervate microgel with marked IgG delivery activity even in the presence of serum. Successful IgG delivery to primary hepatocytes, undifferentiated induced pluripotent stem (iPS) cells, and iPS cell-derived intestinal epithelial cells was also achieved. The construction of complex coacervate microgels with design flexibility and the validity of intracellular IgG delivery with high salt stability were thus demonstrated.

Lidocaine nebulization for airway topical anesthesia can be improved by diminish ex-cannula lost and alkalization

Lidocaine nebulization is noninvasive, safe, and easy to perform. However, it does not provide adequate anesthesia due to the following reasons: 1. There is a high wastage of lidocaine aerosol, with at least 70 % of the lidocaine aerosol being lost from the cannula. This loss of lidocaine results in a lower amount of inhaled lidocaine, which is insufficient to provide adequate anesthesia. 2. The commercial lidocaine preparation has a low penetrating potency. The onset of anesthesia is directly related to the amount of local anesthetic in the lipid-soluble form. However, there are only a few lipid-soluble prototypes in the commercially available lidocaine cartridges. This is because the lidocaine is purposely formulated as acidic solutions (with pH levels between 3.5 and 5.5) in order to enhance the solubility and stability of the anesthetic salts. To address these issues and improve lidocaine anesthesia potency while reducing wastage, a “Y” type cannula was used for aerosol inhalation. Additionally, 1/5 vol of 5 % sodium bicarbonate solution was added to 2 % lidocaine to enhance the pH value to 7.2. This alkalized lidocaine nebulization provides an effective topical anesthesia for bronchoscopy.

In Situ Growth of Well-Aligned MOF Nanoneedle Arrays into Composite Photothermal Membranes for Solar Desalination.

The solar-driven interfacial evaporation (SDIE) technology serves as a clean and facile approach combining seawater desalination to address water shortage and energy crisis. Recently, porous organic framework materials have aroused great attention, and the development of MOF-based composites with significant performance in photothermal conversion and water activation has become one of the important focuses in this field. In this work, an MOF-based composite photothermal membrane (PON@MOF) was prepared via the in situ growth of metal-organic framework (MOF) nanoneedle arrays induced by a pyridine-based organic polymer nanowire network (PON). The PON@MOF membrane possessed an MOF array layer, a PON-induced layer, and a porous support layer. The PON is rich in coordinated nitrogen atoms for anchoring the metal-ion source, and the main role of the PON layer is to provide favorable nucleation sites and orient in situ growth of well-aligned MOF nanoneedle arrays. With the highly conjugated framework of PON@MOF and the light trapping of the nanoarrays strengthening the photothermal conversion as well as the hydrophilic chemical structure facilitating the decrease of the water evaporation enthalpy, the PON@MOF membrane realizes highly efficient thermal vapor conversion. Under solar irradiation (1.0 kW m-2), PON@MOF demonstrated an evaporation rate of 2.14 kg m-2 h-1 and a solar-to-vapor conversion efficiency of 98.5%. Meanwhile, the PON@MOF membrane has excellent salt resistance and stability, highlighting its potential application in desalination. Overall, this work provides a special idea for the structural design of photothermal composites for solar desalination and freshwater production.

Fabrication of novel casein/oligochitosan nanocomplexes for lutein delivery: Enhanced stability, bioavailability, and antioxidant properties

This study aimed to prepare novel nanocomplexes for delivery of lutein using transglutaminase (TGase)-type glycation of casein. The effect of glycated casein nanoparticles on the environmental stability, bioavailability, and antioxidant properties of lutein was investigated. Glycated casein nanoparticles with uniform distribution and small particle size were successfully prepared by ultrasound technology. The structure analysis revealed intermolecular interactions between lutein and glycated casein, with the complexes having a spherical and stable structure. The fabricated nanoparticles exhibited a high encapsulation efficiency (91.89%) and loading capacity (3.06%) for lutein. TGase-type glycation of casein nanoparticles contributed to the strong thermal stability, pH stability, storage stability, and salt stability. Moreover, glycated casein/lutein nanoparticles exhibited resistance to gastric digestion, rapid intestinal release rate, increased lutein bioavailability, and antioxidant activity under simulated digestion. This study provides key support for the development of glycated casein-based nanoparticles as delivery systems and reinforcing stability of hydrophilic nutraceuticals.

Analysis and characterization of residual salts from lithium carbonate industry: Their potential uses for thermal storage systems

The increasing demand for clean energy and the urgent need to reduce greenhouse gas emissions have led to a growing awareness of the importance of thermal energy storage systems in the diversification of the electric matrix. Sensible heat and latent heat storage are the two main techniques, and the choice of storage system depends on the melting point of the substances and the thermal energy required for the processes. This study focused on waste salts obtained from the production process of lithium carbonate. The thermophysical properties of these salts, including specific heat, density, and thermal stability, were examined through various characterization techniques such as X-ray diffraction, chemical analysis, scanning electron microscopy, thermogravimetry, and differential scanning calorimetry. The results revealed promising thermal properties, chemical stability, and physical availability of the waste salts. Additionally, the study explored the potential benefits of reutilizing these waste salts, such as reducing environmental impact, promoting circular economy principles, and creating new market opportunities for commercial products. Overall, this research provides valuable insights into the thermophysical properties of waste salts from lithium carbonate production. The main results are heat capacity in the solid phase (0.767–3.143 J/g°C) and storable thermal energy (114–1153 TWht). These findings contribute to the design and optimization of thermal energy storage systems, highlighting the potential for sustainable and efficient energy storage solutions in the context of global clean energy transitions.

Influence of Protective Colloids on Calcium Tartrate Stability and the Astringency Perception in a Red Wine.

Calcium tartrate instability in wines has been a neglected topic for many years. However, it seems that this problem is gaining prominence, and the industry welcomes inputs to address this issue. Among the alternatives that winemakers use for tartrate salt stabilization, the addition of authorized protective colloids is one of the best choices because they are easy to apply and have a low energetic cost. In the present study, the same red wine was treated with five different commercially available protective colloids in triplicate. The effectiveness of such colloids on calcium tartrate potential instability was estimated, in addition to their side effects on the phenolic composition of the treated wines and their astringency perception, as assessed by sensory analyses of the treated wine. The results show that, under these trial conditions, carboxymethylcellulose is the best choice for reducing the risk of calcium tartrate precipitation in wine. Moreover, the application of protective colloids to the wines had little effect on their color, phenolic composition, or evolution during one year of bottle storage. Finally, the addition of protective colloids did not impact the astringency intensity, but it influenced the dynamic perception of astringency according to the temporal dominance of sensation analysis.

Unravelling the anionic stability of an ether-based electrolyte with a hard carbon or metallic sodium anode for high-performance sodium-ion batteries

In hard carbon (HC) anodes, elucidating the relationship between the solid electrolyte interphase formation and the solvated Na+ co-intercalation mechanism is crucial, particularly considering different anionic salts in ether-based electrolytes. Here, we comprehensively explore the impact of different anionic salts on the electrochemical performance of HC/Na half-cell and elucidate the underlying mechanism through experimental studies and theoretical calculations. The surface morphology of the HC anode and its interphasial property are further investigated to evaluate the differences endowed by the presence of various anionic salts in diglyme (2G). The HC/Na half-cells with NaPF6-2G and sodium trifluoromethanesulfonate (NaCF3SO3)-2G display superior electrochemical performance with faster kinetics and lower interfacial resistance than those with NaClO4-2G, sodium bis-(fluorosulfonyl) imide (NaFSI)-2G and sodium bis-(trifluoromethanesulfonyl) imide (NaTFSI)-2G. NaClO4-2G forms a relatively thick interphase layer with high resistance at the electrode/electrolyte interface owing to its insufficient stability. NaFSI-2G and NaTFSI-2G exhibit severe side reactions with Na metal, producing a thick interphase layer on the HC surface with high interfacial resistance from excess electrolyte decomposition, thus deteriorating the electrochemical performance. In summary, the study on the stability of different anionic salts in ether-based electrolyte for the HC anode with the intercalation mechanism provides valuable insights for screening appropriate conductive salts for high-performance sodium-ion batteries, especially when considering Na metal counter/reference electrodes.

Untangling individual cation roles in rock salt high-entropy oxides

We unravel the distinct role each cation plays in phase evolution, stability, and properties within the Mg1/5Co1/5Ni1/5Cu1/5Zn1/5O high-entropy oxide (HEO) by integrating experimental findings, thermodynamic analyses, and first-principles predictions. Our approach is through sequentially removing one cation at a time from the five-component high-entropy oxide to create five four-component derivatives. Bulk synthesis experiments indicate that Mg, Ni, and Co act as rock salt phase stabilizers whereas only Mg and Ni enthalpically enhance single-phase rock salt stability in thin film growth; synthesis conditions dictate whether Co is a rock salt phase stabilizer or destabilizer. By examining the competing phases and oxidation state preferences using pseudo-binary phase diagrams and first-principles calculations, we resolve the stability differences between bulk and thin film for all compositions. We systematically explore HEO macroscopic property sensitivity to cation selection employing both predicted and measured optical spectra. This study establishes a framework for understanding high-entropy oxide synthesizability and properties on a per-cation basis that is broadly applicable to tailoring functional property design in other high-entropy materials.

Effect of Physicochemical Properties on the Basic Drug-Acid-Polymer Interactions and Miscibility in PVA Based Orodispersible Films.

Salts of weakly basic drugs can partially dissociate in formulations, to give basic drugs and counter acids. The aim of the present study was to clarify the effect of physicochemical properties on the basic drug-acid-polymer interactions and salt-polymer miscibility, and to explain the influence mechanism at the molecular level. Six maleate salts with different physicochemical properties were selected and PVA was used as the film forming material. The relationship between the physicochemical properties and the miscibility was presented with multiple linear regression analysis. The existence state of salts in formulations were determined by XRD and Raman imaging. The stability of salts was characterized by NMR and XPS. The intermolecular interactions were investigated by FTIR and NMR. The results showed that the salt-PVA miscibility was related to polar surface area of salts and Tg of free bases, which represented hydrogen bond interaction and solubility potential. The basic drug-acid-PVA intermolecular interactions determined the existence state and bonding pattern of the three molecules. Meanwhile, the decrease of the stability after formulation increased the number of free bases in orodispersible films, which in turn affected the miscibility with PVA. The study provided references for the rational design of PVA based orodispersible films.

Study on the synergistic action of β-cyclodextrin and sodium caseinate to stabilize the seal oil pickering emulsion

In order to explore the synergistic action of β-cyclodextrin (β-CD) and sodium caseinate (SC) to stabilize the seal oil Pickering emulsion. Seal oil emulsions were prepared by β-CD (β-CD-E), SC (SC-E) and hybrid particles (β-CD@SC-E). Appearance and microscopic morphological analysis, particle size, ζ-potential and viscosity were used to characterize the emulsions. Droplets in emulsion stabilized by the hybrid particles were evenly, with smallest particle size (16.31 μm), largest absolute ζ-potential (27.85 mV) and higher apparent viscosity. Then, stability of the emulsions was evaluated by storage stability, centrifugation stability, pasteurization stability and salt stability. The results showed the appearance, microscopic morphology, particle size, creaming index (CI) of β-CD@SC-E were the least affected after storage, centrifugation, pasteurization and different salt concentration treatment. The interaction analysis indicated that blue shift happened in the maximum absorption wavelength, amide I of β-CD@SC. The α-helixes in β-CD@SC transformed to the β-fold and significant changes occurred in the crystal form and microstructure of β-CD@SC. All these results indicated that self-assembly occurred during the binding of β-CD and SC, which changed their original structures and enhanced their emulsification performance. Besides, hydrogen bonding and hydrophobic interaction played the vital roles during the self-assembly.

Advanced one pot photochemical surface modification approach towards graphene materials and their application in dye removal

Carbonaceous materials have shown undisputable promise as adsorbents and catalysts in various applications. The ability to tune key features such as specific surface area and functionality to improve the activity, represents a key advantage. However, this requires the development of general and versatile synthetic methods to deliver these multifunctional materials. This work reports a convenient general approach to prepare a series of graphene-chromophore systems. Two photochemical methods involving a step-by-step procedure and a one-pot method were compared. It was found that the two-step procedure is limited by the stability of the diazonium salts and thus has a limited application. The one-pot method allows preparation of a wide range of different composites in an easy and inexpensive manner. Synthesised samples were characterised by a range of methods including electron microscopy, X-ray diffraction, infra-red spectroscopy and gas adsorption. Transmission electron microscopy analysis revealed an ordered array of chromophores on the surface of the graphene nanoplatelets. The samples were tested as potential materials for dye removal; these studies revealed that most graphene-chromophore materials can successfully remove organic pollutants such as methylene blue, rhodamine B and methyl orange from aqueous media.

Maleic anhydride-functionalized cellulose nanocrystal-stabilized high internal phase Pickering emulsion for pesticide delivery

The salt-responsiveness of Pickering emulsions has significantly influenced their applications due to the large amount of salt on the surface of plant leaves. The present study provided a maleic anhydride-functionalized cellulose nanocrystal-stabilized high internal phase Pickering emulsion (MACNCs-HIPPEs) that was stable to high-concentration salt and used for pesticide delivery. The stability of MACNCs-HIPPEs was investigated by adjusting the oil-phase volume fraction (φ), the MACNCs concentration, NaCl dosages, and the rheological properties. The high internal phase Pickering emulsion was obtained at φ of 0.8 and MACNCs concentration of 2wt% and showed excellent salt stability (NaCl, 1200 mM) and significant storage stability (60 days). The sustained release of imidacloprid (IMI) from imidacloprid-loaded MACNCs-HIPPEs (IMI@MACNCs-HIPPEs) showed a positive correlation to the temperature (15°C, 25°C, 35°C), indicating clear thermo-responsiveness of the prepared pesticide formulation. The test of spread and retention of IMI@MACNCs-HIPPEs on the leaf surface showed a significant advantage compared with the commercial IMI water dispersible granules (CG). All the advantages mentioned above showed the excellent potential of the MACNCs-HIPPEs in delivering lipophilic pesticides.

Tailoring anionic solar evaporator with an enhanced Donnan effect for a highly effective salt resistance desalination and water purification

Emerging solar-driven interfacial water evaporation demonstrates immense potential in mitigating worldwide water shortages, offering exceptional solar-to-vapor conversion efficiency, off-grid operability, zero liquid discharge capability and low carbon footprint. A critical requirement for sustainable extraction clean water from brine is the development of solar evaporators with both salt resistance and high evaporation rates. In response to this demand, this research proposed an enhanced Donnan effect anionic solar evaporator through filling wood in situ with PVA/PAA hydrogel. The resulting anionic solar evaporator demonstrated broadband spectral absorption, excellent photothermal conversion, and water activation capability. Notably, based on the negative charge property of the –COO– group anionic hydrogel, it could enhance Donnan effect and restrict the diffusion of Cl− to the evaporator, ensure enduring salt resistance and stability in purifying brine effectively. Experiments proved that the anionic anionic solar evaporator attained a remarkable water evaporation rate of 2.439 kg m−2 h−1 during a desalination of 15 wt% NaCl solution under 1 kW m−2 solar radiation, and no obvious salt accumulation had been observed during prolonged evaporation processes. With high efficiency, renewability, deployability, low cost, and durability, the anionic solar evaporator emerges as a promising solution for mitigating water scarcity, especially in economically challenged regions and provides valuable perspectives for future investigations into the water-energy-climate nexus.

Low Fouling Polyelectrolyte Layer-by-Layer Self-Assembled Membrane for High Performance Dye/Salt Fractionation: Sequence Effect of Self-Assembly.

Layer-by-layer (LbL) self-assembly of oppositely charged polyelectrolytes (PEs) is usually performed on a conventional ultrafiltration base substrate (negative zeta potential) by depositing a cationic PE as a first layer. Herein, we report the facile and fast formation of high performance molecular selective membrane by the nonelectrostatic adsorption of anionic PE on the polyvinylidene fluoride (PVDF, zeta potential -17 mV) substrate followed by the electrostatic LbL assembly. Loose nanofiltration membranes have been prepared via both concentration-polarization (CP-LbL, under applied pressure) driven and conventional (C-LbL, dipping) LbL self-assembly. When the first layer is poly(styrene sodium) sulfonic acid, the LbL assembled membrane contains free -SO3- groups and exhibits higher rejection of Na2SO4 and lower rejection of MgCl2. The reversal of salt rejection occurs when the first layer is quaternized polyvinyl imidazole (PVIm-Me). The membrane (five layers) prepared by first depositing PStSO3Na shows higher rejection of several dyes (97.9 to >99.9%), higher NaCl to dye separation factor (52-1800), and higher dye antifouling performance as compared to the membrane prepared by first depositing PVIm-Me (97.5-99.5% dye rejection, separation factor ∼40-200). However, the C-LbL membrane requires a longer time of self-assembly or higher PE concentration to reach a performance close to the CP-LbL membranes. The membranes exhibit excellent pressure, pH (3-12), and salt (60 g L-1) stability. This work provides an insight for the construction of low fouling and high-performance membranes for the fractionation of dye and salt based on the LbL self-assembly sequence.

Studies on the Properties and Stability Mechanism of Double Emulsion Gels Prepared by Heat-Induced Aggregates of Egg White Protein-Oligosaccharides Glycosylation Products.

Multiple emulsions can dissolve some substances with different properties, such as hydrophilicity and lipophilicity, into different phases. They play an important role in protection, controlled release and targeted release of the encapsulated substances. However, it's poor stability has always been one of the main problems restricting its application in the food industry. For this reason, a heat-induced aggregate (HIA) of Maillard graft product of isomalto-oligosaccharides (IMO), as well as egg white protein (EWP), was used as hydrophilic emulsifier to improve the stability of W1/O/W2 emulsions. Moreover, gelatin was added into the internal aqueous phase (W1) to construct W1/O/W2 emulsion-gels system. The encapsulation efficiency of HIA-stabilized W1/O/W2 emulsions remained nearly unaltered, dropping by only 0.86%, significantly outperforming the conjugates and physical mixture of IMO and EWP in terms of encapsulation stability. The emulsion-gels system was constructed by adding 5% gelatin in the W1, and had the highest EE% and good salt and heat stability after 30 days of storage. This experiment provides guidance for improving the stability of W1/O/W2 emulsions system and its application in the package delivery of functional substances in the food field.

Milk-derived antimicrobial peptides incorporated whey protein film as active coating to improve microbial stability of refrigerated soft cheese

Nisin is the first FDA-approved antimicrobial peptide and shows significant antimicrobial activity against Gram-positive bacteria, but only a weakly inhibitory effect on Gram-negative bacteria. The aim of this study was to prepare whey protein-based edible films with the incorporation of milk-derived antimicrobial peptides (αs2-casein151–181 and αs2-casein182–207) and compare their mechanical properties and potential application in cheese packaging with films containing nisin. These two antimicrobial peptides showed similar activity against B. subtilis and much higher activity against E. coli than bacteriocin nisin, representing that these milk-derived peptides had great potential to be applied as food preservatives. Antimicrobial peptides in whey protein films caused an increase in film opaqueness and water vapor barrier properties but decreased the tensile strength and elongation at break. Compared to other films, the whey protein film containing αs2-casein151–181 had good stability in salt or acidic solution, as evidenced by the results from scanning electron microscope and Fourier transform infrared spectroscopy. Whey protein film incorporated with αs2-casein151–181 could inhibit the growth of yeasts and molds, and control the growth of psychrotrophic bacteria present originally in the soft cheese at refrigerated temperature. It also exhibited significant inhibitory activity against the development of mixed culture (E. coli and B. subtilis) in the cheese due to superficial contamination during storage. Antimicrobial peptides immobilized in whey protein films showed a higher effectiveness than their direct application in solution. In addition, films containing αs2-casein151–181 could act as a hurdle inhibiting the development of postprocessing contamination on the cheese surface during the 28 days of storage. The films in this study exhibited the characteristics desired for active packaging materials.

Investigation of Earth-Abundant Metal Salts for the Inhibition of Asphalt-Derived Volatile Organic Compounds.

Asphalt is used globally in construction for roads, pavements, and buildings; however, as a fossil-derived material, it is known to generate volatile organic compounds (VOCs) upon exposure to heat and light that can be harmful to human health. Several heterogeneous strategies have been reported for the inhibition of these VOCs; however, the direct use of inexpensive, accessible Earth-Abundant metals has not been extensively explored. In this study, simple metal salts are examined for their coordination capability toward asphalt-derived VOCs. From UV-visible (UV-vis) spectroscopic studies, FeCl3 emerged relative to other metal salts (metal = Mn, Co, Ni, Cu, Zn) as a promising candidate for the adsorption and retention of Lewis basic compounds. Coordination of an example oxygen-containing VOC, benzofuran (Bf), to Fe yielded a paramagnetic semi-octahedral complex Fe(Bf)3Cl3. Evaluation by thermal gravimetric analysis (TGA) coupled to infrared spectroscopy (IR) demonstrated that the complex was stable up to 360 °C. Spectroscopic evaluation demonstrated the stability of the complex upon visible light irradiation and in the presence of a variety of organic pollutants. The potential application of Fe was demonstrated by subjecting biochar to FeCl3 followed by the addition of Bf. It was discovered that this Fe-rich biochar was successful at adsorbing Bf suggesting the possibility of introducing Fe to biochar late-stage in processing to deter asphalt degradation and VOC emissions. An understanding of the binding and stability of Fe salts to VOCs provides insight into how a sustainable infrastructure can be achieved.

Development of a consistent geochemical model of the Mg(OH)2–MgCl2–H2O system from 25°C to 120°C

The formation of magnesium chloride-hydroxide salts (magnesium hydroxychlorides) has implications for many geochemical processes and technical applications. For this reason, a thermodynamic database for evaluating the Mg(OH)2–MgCl2–H2O ternary system from 0 °C–120 °C has been developed based on extensive experimental solubility data. Internally consistent sets of standard thermodynamic parameters (ΔGf°, ΔHf°, S°, and CP) were derived for several solid phases: 3 Mg(OH)2:MgCl2:8H2O, 9 Mg(OH)2:MgCl2:4H2O, 2 Mg(OH)2:MgCl2:4H2O, 2 Mg(OH)2:MgCl2: 2H2O(s), brucite (Mg(OH)2), bischofite (MgCl2:6H2O), and MgCl2:4H2O. First, estimated values for the thermodynamic parameters were derived using a component addition method. These parameters were combined with standard thermodynamic data for Mg2+(aq) consistent with CODATA (Cox et al., 1989) to generate temperature-dependent Gibbs energies for the dissolution reactions of the solid phases. These data, in combination with values for MgOH+(aq) updated to be consistent with Mg2+-CODATA, were used to compute equilibrium constants and incorporated into a Pitzer thermodynamic database for concentrated electrolyte solutions. Phase solubility diagrams were constructed as a function of temperature and magnesium chloride concentration for comparisons with available experimental data. To improve the fits to the experimental data, reaction equilibrium constants for the Mg-bearing mineral phases, the binary Pitzer parameters for the MgOH+ — Cl− interaction, and the temperature-dependent coefficients for those Pitzer parameters were constrained by experimental phase boundaries and to match phase solubilities. These parameter adjustments resulted in an updated set of standard thermodynamic data and associated temperature-dependent functions. The resulting database has direct applications to investigations of magnesia cement formation and leaching, chemical barrier interactions related to disposition of heat-generating nuclear waste, and evaluation of magnesium-rich salt and brine stabilities at elevated temperatures.

Base-Driven Ring-Opening Reactions of Vinylene Carbonate

Vinylene carbonate (VC) is the most commonly applied performance-enhancing electrolyte additives in Li-ion batteries to date. Despite numerous studies, there is a lack of consensus regarding the various reaction pathways of VC and their implications. VC has primarily been observed to either polymerize forming poly(vinylene carbonate) (poly(VC)) or decompose releasing major amounts of CO2, two seemingly contradictory processes. Herein, we present evidence of additional reaction pathways of VC highlighting its role as a H2O scavenging agent. In contrast to the typical electrolyte solvent ethylene carbonate, VC reacts much more rapidly with water impurities, especially when in contact with hydroxides, forming products less likely to influence cell performance. Efficient removal of water and hydroxides is essential to preserve the stability of Li-ion electrolyte solvent and salt, hence guaranteeing a long lifetime of the battery. Model studies pinpointing reaction pathways of electrolytes and additives, as presented herein, are critical not only to improve modern Li-ion cells but also to establish design principles for future battery chemistries.

Preparation of protein-stabilized Litsea cubeba essential oil nano-emulsion by ultrasonication: Bioactivity, stability, in vitro digestion, and safety evaluation

Litsea cubeba essential oil (LCEO) has garnered widespread attention due to its robust biological activity. However, challenges such as high volatility, limited water solubility, and low bioavailability impede its application. Nano-emulsion encapsulation technology offers an effective solution to these issues. In this study, we prepared litsea cubeba essential oil nano-emulsion (LCEO-NE) for the first time using whey protein (WP) as the emulsifier through an ultrasonic-assisted method, achieving high efficiency with minimal energy consumption. Transmission electron microscopy and dynamic light scattering analyses revealed that the nanoparticles were uniformly spherical, with a particle size of 183.5 ± 1.19 nm and a zeta potential of −35.5 ± 0.95 mV. Stability studies revealed that LCEO-NE exhibited excellent thermal and salt stability, maintaining its integrity for up to four weeks when stored at 4 °C and 25 °C. In vitro digestion assays confirmed the digestibility of LCEO-NE. Furthermore, evaluation of the DPPH, ABTS, and antimicrobial activities revealed that LCEO-NE displayed superior bacteriostatic and antioxidant properties compared to LCEO. Scanning electron microscopy elucidated that its bacteriostatic effect involved the disruption of bacterial microstructure. Hemocompatibility and cytotoxicity assays demonstrated the safety of LCEO-NE within the effective concentration range. This research supports the utilization of nanoparticles for encapsulating LCEO, thereby enhancing its stability and bioactivity, and consequently expanding its applications in the food and pharmaceutical industries.