Adsorption Of Nanoparticles Research Articles

Synthesis of Aluminum Oxide Nanoparticle Adsorbents from Waste Aluminum Foil and Assesses Their Efficiency in Removing Lead (II) Ions from Water

Synthesis of Aluminum Oxide Nanoparticle Adsorbents from Waste Aluminum Foil and Assesses Their Efficiency in Removing Lead (II) Ions from Water

Toward an Enhanced Hydrophilic TiO2 Nanoparticles Adsorption at Air-Liquid Interface Through Ion Regulation.

This study investigates the dynamic properties of air-liquid interfacial tension for hydrophilic TiO2 P25 utilizing the pendant drop method. Additionally, it examines the interfacial adsorption mechanism of hydrophilic TiO2 particles, considering the characteristics of particle surface charge distribution in relation to ion regulation to enhance particle interface adsorption. Experimental results reveal that in the absence of ion addition, the TiO2 P25 suspension system exhibits limited interfacial adsorption due to its superhydrophilicity, regardless of particle concentration. The addition of NaCl increases the surface charge density of the particles, strengthens the electrostatic attraction between particles and the interface, and enhances particle adsorption. Specifically, at a low NaCl concentration (0.01 wt %), the increased surface charge density and contact angle of the particles elevate particle activity and high interfacial packing density. At a higher NaCl concentration (0.1 wt %), while NaCl further increases the particle contact angle, the increased effective cross-sectional area of the air-liquid interface occupied by individual particles leads to a reduction in surface free energy. Despite the enhanced electrostatic attraction, this results in a lower packing density.

Size-Dependent Electrostatic Adsorption of Polymer-Grafted Gold Nanoparticles on Polyelectrolyte Brushes.

Designing a functional surface that selectively adsorbs nanoparticles based on their size and shape is essential for developing an advanced adsorption-based, postsynthesis nanoparticle separation device. We demonstrate selective adsorption of larger nanoparticles from solution onto a polyelectrolyte brush by tuning the salt concentration. Specifically, a positively charged polyelectrolyte brush is created by converting pyridine groups of poly(2-vinylpyridine) to n-methylpyridinium groups using methyl iodide. The adsorption kinetics and thermodynamics of poly(ethylene glycol)-grafted, negatively charged gold nanoparticles (diameters of 12 and 20 nm) were monitored as a function of salt concentration. In a salt-free solution, the polyelectrolyte brush adsorbs gold nanoparticles of both sizes. As the salinity increases, the areal number density of adsorbed nanoparticles monotonically decreases and becomes negligible at high salinity. Interestingly, there is an intermediate range of salt concentrations (i.e., 15-20 mM of NaCl) where the decrease in nanoparticle adsorption is more pronounced for smaller particles, leading to size-selective adsorption of the larger nanoparticles. As a further demonstration of selectivity, the polyelectrolyte brush is immersed in a binary mixture of 12 and 20 nm nanoparticles and found to selectively capture larger particles with ∼90% selectivity. In addition, the size distribution of as-synthesized gold nanoparticles, with an average diameter of 12 nm, was reduced by selectively removing larger particles by exposing the solution to polyelectrolyte brush surfaces. This study demonstrates the potential of a polyelectrolyte brush separation device to remove larger nanoparticles by controlling electrostatic interactions between polymer brushes and particles.

Stable Au(111) Hexagonal Reconstruction Induced by Perchlorinated Nanographene Molecules.

Surface reconstructions play a crucial role in surface science because of their influence on the adsorption and arrangement of molecules or nanoparticles. On the Au(111) surface, the herringbone reconstruction presents favorable anchoring at the elbow sites, where the highest reactivity is found. In this work, we deposited large organic perchlorinated molecules on a Au(111) surface via high-vacuum electrospray deposition. With noncontact atomic force microscopy measurements at room temperature, we studied the molecular structures formed on the surface before and after annealing at different temperatures. We found that a supramolecular layer is formed and that a hexagonal reconstruction of the Au(111) surface is induced. After high-temperature annealing, the molecules are removed, but the hexagonal Au(111) surface reconstruction is preserved. With the hexagonal Au(111) surface reconstruction, a periodic lattice of anchoring sites is formed.

Defect-Selective Energy Barrier Crossing during Adsorption of Colloidal Gold Nanoparticles on Zinc Sulfide Crystals under Overall Electrostatic Repulsion

Defect-Selective Energy Barrier Crossing during Adsorption of Colloidal Gold Nanoparticles on Zinc Sulfide Crystals under Overall Electrostatic Repulsion

Synthesis of MIPs@H2S Nanoparticle Adsorbent for the Specific Adsorption of Hazardous Hydrogen Sulfide Gas: Approach to Optimization

Synthesis of MIPs@H2S Nanoparticle Adsorbent for the Specific Adsorption of Hazardous Hydrogen Sulfide Gas: Approach to Optimization

Enhanced colorimetric analysis substrate based on graphene oxide open-close actuator

Traditional colorimetric sensors often suffer from low color resolution and insufficient sensitivity. Therefore, for colorimetric detection to serve as a reliable quantitative analysis technique, an enhanced substrate with high sensitivity and repeatability is required. This strategy employs an interfacial network constructed between two-dimensional graphene oxide (GO) lamellar structures to create a substrate for colorimetric analysis. Under normal conditions, the newly synthesized GO inhibits oxidative activity due to van der Waals forces between the lamellar interfaces, resulting in the GO actuator being in the closed state. During Ag+ colorimetric analysis, the GO interlayer adsorption of silver nanoparticles (AgNPs) disrupts the interlayer van der Waals forces, releasing its oxidase activity and significantly enhancing Ag+ oxidation. The resulting actuator exhibits a faster driving speed (0.045 μM/s), excellent sensitivity, and stability. Additionally, the reducing properties of dopamine (DA) can be utilized to encapsulate the GO actuator with polydopamine, closing the GO actuator. Similarly, the reducing property of ascorbic acid (AA) can be utilized to restore the GO actuator to a closed state. These distinct reduction mechanisms allow for an effective visual distinction between AA and DA. With these advantages, the actuator can be developed into simple analytical tools (such as Ag+ colorimetric test strips and DA and AA test kits), demonstrating significant potential for practical application.

Enhanced hydrophobic properties, wear and corrosion resistance of plasma electrolyte oxidation coatings on AZ31B magnesium alloys with addition of TiO2 nanoparticles

Nanocomposite coatings were fabricated on AZ31B magnesium alloy by means of plasma electrolyte oxidation (PEO) with the addition of TiO2 nanoparticles into the alkaline electrolyte, followed by low surface energy modification in the ethanol solution of lauric acid. The dual-layered nanocomposite PEO coatings composed of MgO, Mg2SiO4, anatase-TiO2, rutile-TiO2, and Mg2TiO4 were formed, and the TiO2 nanoparticles incorporated into the PEO coatings via both inertia and reactive modes. Besides, the penetration and adsorption of TiO2 nanoparticles created a distribution gradient in the coating thickness direction. The wear rate of the PEO coatings with TiO2 nanoparticles in 4 g/L was approximately 82 % lower than that of the bare substrate and approximately 39 % lower than that of the PEO coatings without TiO2 addition, respectively. The enhancement in wear resistance was due to the synergistic effect of the lower coefficient of friction (COF), the higher microhardness and the denser microstructure with finer micropores and less microcracks on the coatings than that of the TiO2-free coatings. Besides, the hydrophobic property was enhanced for the low surface energy modified PEO coatings with the addition of TiO2 nanoparticles in the electrolyte. Moreover, a significant enhancement in the corrosion resistance was achieved for the PEO coating with the addition of TiO2 nanoparticles in 4 g/L. It exhibited a higher corrosion inhibition efficiency and a lower corrosion rate than that in other concentrations and without TiO2 addition. The improvement in anti-corrosion property was originated from the formation of phases including TiO2 and Mg2TiO4 in the coating, and denser microstructure with better hydrophobic properties for the PEO coatings with TiO2 nanoparticles in 4 g/L compared with that in other concentrations. Accordingly, the hydrophobic, wear-resistant and corrosion-resistant PEO coatings with TiO2 nanoparticles exhibited significant advantages in the field of Mg alloys protection.

Synthesis of 1,2,4-triazole-based deep eutectic solvents modified nickel ferrite nanoparticles and their application in dispersive solid phase extraction of triazole pesticides prior to LC-MS/MS analysis

A dispersive solid phase extraction method using new magnetic nanoparticles based on nickel ferrite was introduced for the extraction of six triazole pesticides (penconazole, hexaconazole, tebuconazole, diniconazole, triadimefon, and difenoconazole) from water samples before liquid chromatography-tandem mass spectrometry analyses. Initially, a new deep eutectic solvent was synthesized with 1,2,4-triazole and n-octanol for surface modification of the nanoparticles easily achieved through microwave radiation. The nanoparticles morphology, magnetic properties, adsorption capacity, isotherms, and crystalline patterns of the sorbent were examined. The capability of the sorbent was evaluated by extracting the target pesticides from water samples showing significant differences in adsorption capacity and efficiency between the modified and non-modified nanoparticles. High extraction recoveries (68-86%) were achieved for the analytes using small amounts of the sorbent with low limits of detection (0.03-0.08 ng mL-1) and quantification (0.13-0.29 ng mL-1), a wide linear range (0.29-250 ng mL-1), and acceptable precision (relative standard deviations ≤6.9%).

Organic matter excreted by the protozoan Tetrahymena thermophila and its effects on the bioaccumulation of nanoparticles

Although organic matter (exudate) excreted by aquatic organisms is an important component of dissolved organic matter (DOM) in the natural environment, its potential effects on the bioaccumulation of nanoparticles (NPs) remain unclear. In the present study, we examined the effects of the exudates from the protozoan Tetrahymena thermophila on the bioaccumulation (including uptake and cell surface adsorption) of iron oxide (Fe2O3, polyacrylate coated) and silica (SiO2) NPs in T. thermophila. The exudates were mostly (93.6%, in carbon) composed of < 1-kDa molecules (e.g., lipids). When the exudates were mixed with the NPs, significant adsorption occurred on SiO2 NPs but not on Fe2O3 NPs. Independent of their adsorption by the NPs, the exudates significantly inhibited the bioaccumulation of both SiO2 NPs and Fe2O3 NPs by T. thermophila. This inhibitory effect was shown to be mainly due to their inhibition of NP adsorption on the cell surface. By contrast, the exudates had negligible effects on the uptake of either NP type, most likely due to their low molecular weight. Since DOM in the aquatic environment is dominated by molecules < 1kDa, the potential effects of low-molecular-weight DOM, such as exudates from aquatic organisms, on the bioaccumulation of NPs merits greater attention. Environmental ImplicationNanoparticles (NPs) are hazardous materials widespread in the natural environment. Previous studies showed that dissolved organic matter (DOM) in aquatic environments determine the environmental behavior and ecological effects of NPs. Although organic matter (exudate) excreted by aquatic organisms is an important component of DOM, its potential effects on the bioaccumulation of NPs remain unclear. In the present study, we found that the exudates inhibited the cell-surface adsorption of NPs but had no effects on NP uptake, as different from the well-known effects of DOM on NP bioaccumulation. This finding merits attention during evaluations of the environmental risks of NPs.

Preparation of Alkali-Resistant Lignin Nanospheres Loaded with Silver Nanoparticles and Their Applications Toward Antibiosis and Printing.

Lignin nanoparticles (LNPs) loaded with silver nanoparticles have exhibited significant application potential in antibacterial and catalytic fields. However, the high solubility of LNPs in silver ammonia solution makes it difficult to achieve the reduction of Ag+ and the adsorption of silver nanoparticles. In this study, a protecting agent, terephthalic aldehyde (TA) is used to block lignin condensation and introduce aldehyde groups onto the lignin molecular backbone during lignin extraction. Furthermore, the TA stabilized lignin (TASL) is cross-linked with bisphenol A diglycidyl ether (BADGE) to enhance its alkali resistance performance and subsequently prepared into alkali-resistance BADGE- TASL hybrid LNPs (BADGE- TASL hy-LNPs) by anti-solvent precipitation and self-assembly. Because the presence of a large number of aldehyde groups in TASL compensates for the loss of phenolic hydroxyl groups caused by crosslinking reactions, a high loading of silver nanoparticles of 54.00% is obtained after redox reaction and adsorption in silver ammonia solution. When the BADGE-TASL hy-LNPs@Ag is used as an antibacterial agent, its inhibition efficiency reached ≈99%. Besides, the BADGE-TASL hy-LNPs@Ag can serve as a printing material for the preparation of conductive printing ink. Therefore, this study provides a strategy for lignin functionalization and application in printed electronics and antimicrobial fields.

Adsorption and Photocatalytic of Biosynthesis Zinc Ferrite Nanoparticles for Removing Acid Black 210 Dye from Aqueous Medium

عالجت هذه الدراسة مياه الصرف الصحي الملوثة بصبغة حمض الأسود 210 عن طريق تقنية الامتزاز والتحفيز الضوئي باستخدام جزيئات الزنك الفريت النانوية. تم تشكيل جسيمات الزنك الفريت النانوية بتقنية التخليق الأخضر باستخدام أوراق الأوكالبتوس كعامل اختزال. المسح المجهري للإلكترون ، الأشعة السينية المشتتة للطاقة ، حيود الأشعة السينية ، Brunauer-emmett -teller ، مقياس زيتا. أشارت الصور من SEM إلى التبلور والشكل الكروي للجسيمات النانوية المصنوعة من الفريت الزنك بحجم جسيم يبلغ 32 نانومتر. بالإضافة إلى ذلك ، تضمنت هذه الدراسة استخدام مفاعل ضوئي لإنجاز عملية التحلل الضوئي. تم فحص تأثير العوامل الرئيسية على الامتزاز و التحلل الضوئي للصبغة. بناءً على نتائج الامتزاز ، كانت فعالية إزالة الصبغة بعد 180 دقيقة 74٪ في الظروف المثلى 5 غم / لتر ، 0.75 غم / لتر ، 5 ، 45 درجة مئوية لتركيز AB210 ، جرعة الجسيمات النانوية الفريت الزنك ، ودرجة الحموضة ، ودرجة الحرارة ، على التوالى. في المقابل ، أظهرت نتائج التحلل الضوئي أنه تمت إزالة خمسة ملغم / لتر من الصبغة بالكامل في غضون 30 دقيقة عند درجة الحموضة المثلى 7 ، وشدة الأشعة فوق البنفسجية 24 واط / م2 ، ودرجة حرارة 45 درجة مئوية. تمت دراسة متساوي درجة حرارة الامتزاز باستخدام نماذج Freundlich و Langmuir و Temkin و Dubinin .

Entropy-favorable adsorption of polymer-grafted nanoparticles at fluid-fluid interfaces.

The adsorption of polymer-grafted nanoparticles at interfaces is a problem of fundamental interest in physics and soft materials. This adsorption behavior is governed by the interplay between interaction potentials and entropic effects. Here, we use molecular dynamics simulations and umbrella sampling methods to study the adsorption behavior of a Janus-like homopolymer-grafted nanoparticle at fluid-fluid interfaces. By calculating the potential of the mean force as the particle moves from fluid A to the interface, the adsorption energy Ea can be obtained. When two homopolymer chains with types A and B are grafted to the opposite poles of the particle, Ea shows a scaling behavior with respect to chain length N: Ea ∝ N0.598. This is determined by the interactions between polymers and fluids. The enthalpy dominates, and the entropy effects mainly come from the rotational entropy loss of the polymer-grafted nanoparticle at interfaces, which disfavors the stabilization of particles at interfaces. When the grafted polymer number m is large, the adsorption energy exhibits a linear dependence on m. While the enthalpy dominates the behavior, the entropy becomes significant at a larger chain length of N = 15, where the configurational entropy of the polymer chains dominates the entropy of the system. The globule-coil transition occurs when polymers move from poor solvents to good solvents, increasing the configurational entropy and favoring the stabilization of particles at interfaces. Our study provides novel insights into the stabilization mechanism of polymer-grafted nanoparticles at interfaces and reveals the stabilization mechanism favored by the configurational entropy of grafted polymer chains.

Effect of solvothermal reaction time on adsorption and photocatalytic activity of spinel ZnFe2O4 nanoparticles

The present investigation explored the impact of solvothermal reaction time on the adsorption properties of synthesized spinel ZnFe2O4 Nanoparticles (ZF NPs) and their photocatalytic activity for the degradation of congo red (CR) dye. The structure, morphology and chemical composition is identified for the synthesized ZF NPs. The reaction times for the solvothermal synthesis of ZF NPs were investigated at time intervals of 6 hrs and 18 hrs which are denoted as ZF-6 h and ZF-18 h respectively. The XRD confirms the formation of spinel-type ZF-6 h and ZF-18 h with crystallite size of 5.50 nm and 8.36 nm for ZF-6 h and ZF-18 h respectively. The FESEM image of ZF-6 h exhibits microspheres, whereas in ZF-18 h NPs, the microspheres undergoes deformation. TEM analysis of ZF-6 h revealed that the microspheres were consists of 8–10 nm size ZF-NPs. Raman spectroscopy and XPS studies indicates, the reaction time influence the occupancy with 64 % and 32 % of inversion of Zn2+ cations from tetrahedral to octahedral sites in ZF-6 h and ZF-18 h, respectively. The surface area of mesoporous ZF-6 h and ZF-18 h are 138.29 m2/g and 128.41 m2/g respectively as confirmed using BET and BJH techniques. The CR dye adsorption capacity of 123.73 mg/g for ZF-6 h is higher compared to ZF-18 h (99.93 mg/g). The maximum dye removal efficiency evaluated for ZF-6 h NPs and ZF-18 h NPs was 87.33 % and 73.09 % respectively upon exposure of natural sunlight. The recyclability study identifies that ZF-6 h NPs remain stable for three degradation cycles. These results indicate that reaction time in solvothermal synthesis is sensitive to the morphology and physicochemical properties of ZF NPs. The enhanced performance of such ZF NPs is attributed to the synergistic effect of adsorption followed by photocatalytic (photo-Fenton) degradation of dyes.

Novel Triton X-114 coated Fe3O4 magnetic nanoparticle adsorbent for Cd(II) and Co(II) ions preconcentration in honey samples using magnetic solid-phase extraction: Determination by ICP-OES

This work focuses on creating and studying the effectiveness of Fe3O4 nanoparticles coated with (3-aminopropyl)triethoxysilane (APTES) and polyethylene glycol tert-octylphenyl ether (TX-114), respectively, as adsorbent. Fe3O4@APTES@TX-114 adsorbent extracts heavy metal cations Cd2+ and Co2+ using a magnetic solid phase extraction technique. The synthesized magnetic nanoparticles (MNPs) were characterized by Field Emission Scanning Electron Microscope (FESEM), Energy Dispersive X-Ray Analysis (EDX), Fourier Transform Infrared Spectroscopy (FT-IR), and Thermogravimetric Analysis (TGA). After this stage, Cd2+ and Co2+ determinations were made with the ICP-OES device. The optimum conditions for recovering Cd2+ and Co2+ cations were pH 7, an adsorbent dosage of 2 g/L, and a contact time of 120 min. While the method was compatible with Langmuir and Freundlich isotherm models, the pseudo-second-order kinetic equation was more compatible than the pseudo-first-order. Acidic and basic media were investigated for the desorption of Cd2+ and Co2+ ions from the adsorbent. At the same time, maximum recovery was achieved for both cations at a concentration of 1.5 mol/L HCl, but no significant recovery was obtained in the NaOH medium. The common ion study observed that Cd2+ and Co2+ cations were recovered over 95 % in the presence of many cations and anions at different concentrations. The relative standard deviation (RSD), limit of quantification (LOQ), limit of detection (LOD), and enrichment factor (EF) were calculated as 1.40 %, 2.963 µg/L, 0.889 µg/L, 20.99 for Cd2+ and 3.05 %, 1.88 µg/L, 0.564 µg/L, 109.41 for Co2+, respectively. The magnetic solid phase extraction method realized quantitative recovery of Cd2+ and Co2+ cations in different honey samples. It was found that the heavy metal contents in honey samples from the Sakarya region are below permissible levels.

Unraveling the Complexities of Silica Nanoparticle Adsorption onto Polymer Latexes in Pickering Emulsion Polymerization.

Incorporating unmodified silica nanoparticles onto polymer latexes to fabricate aqueous polymer dispersions without relying on electrostatic attraction during the Pickering emulsion polymerization process still faces challenges. For negatively charged silica nanoparticles to successfully adsorb onto polymer latexes, particularly in an anionic initiator emulsion polymerization system, they have remained elusive without the use of auxiliary monomers and cationic initiators. This study investigates various experimental parameters, such as emulsion polymerization temperature, monomer solubility, salt concentration, and cation type, to elucidate the factors influencing the adsorption of unmodified silica nanoparticles in Pickering emulsion polymerization. While poly(methyl methacrylate) (PMMA)/SiO2 hybrid latexes can be obtained under pH conditions of 5-6 and at temperatures of 65 °C or below, the loading rate of silica nanoparticles decreases as the reaction temperature increases, resulting in bare PMMA latexes without silica nanoparticle adsorption at temperatures exceeding 70 °C. Introducing styrene (St) into the monomer mixture with methyl methacrylate in a ratio of up to 10 wt % leads to a gradual decrease in silica nanoparticle loading rate, from 27.3 to 8.2 wt %, attributed to the low solubility of St in water. Furthermore, the presence of sodium ions (Na+) is found to be crucial for silica nanoparticle adsorption onto PMMA latexes, as the sodium ions have a stabilizing effect on both the silica nanoparticles and the silica nanoparticle-armored latexes. These findings highlight the complex nature of Pickering emulsion polymerization in the presence of unmodified silica nanoparticles, demonstrating that the loading rate of silica nanoparticles onto polymer latexes is influenced by various factors. These insights pave the way for developing aqueous polymer dispersions with high silica nanoparticle loading rates onto polymer latexes, which is a desirable trait in the coating industry.

Effect of silica nanoparticles on crude oil emulsions stabilized by a natural surfactant from Fenugreek Seeds and polyacrylamide for subsurface oil mobilization applications

Emulsions represent a sustainable method for subsurface resource recovery due to their superior performance in pore plugging, mobility control and interfacial tension reduction. However, the stability of emulsion plays a vital role in determining the success of field implementation. In this work, a novel formulation is reported for emulsions wherein they have been stabilized by natural surfactant extracted from fenugreek seed. In this work, two emulsion systems are reported, that is surfactant polymer and nanoparticle-surfactant-polymer emulsion. Surfactant-polymer emulsions are stabilized by natural surfactant whereas nanoparticle-surfactant-polymer emulsion are stabilized in presence of nanoparticle and natural surfactant. Both the emulsions exhibit shear thinning profile as observed from rheological studies. Nanoparticle-surfactant-polymer emulsions were found to be thermally stable than that of Surfactant-polymer emulsions as evident from microscopic and rheological studies. An increase in temperature has the unfavorable impact on surfactant-polymer emulsion as huge drop in viscosity profile was observed. The viscosity profiles of nanoparticle-surfactant-polymer emulsions were found to be best fitted by the Krieger-Dougherty model with the value of coefficient correlation R2 = 0.99. The contact angle studies showed that NSP solution can reduce the contact angle to much lower value, which is 111˚ to 30˚ whereas surfactant-polymer solution was able to reduce from 116˚ to 57˚ only. Adsorption of silica nanoparticle was also observed in presence of sandstone and decrease in 27.32 % of peak absorbance was observed in span of 20 days. Therefore, finding of the study indicates that nanoparticle-surfactant-polymer emulsions has potential to perform better than surfactant-polymer emulsions, even at elevated temperature, and can be a better and cost-effective alternative to the conventional emulsions used in oilfield applications.

Adsorption of Colloidal Nanoparticles to Supports: Employing Electrostatic Charge Screening and Barrierless Self-Assembly as Nanointegration Strategy.

Surfactant-free nanoparticles can be adsorbed on a support material by electrostatic deposition which requires electrostatic attraction between the nanoparticles and the support material. However, when nanoparticles and support have a similar isoelectric point (IEP), it is difficult to create such electrostatically attractive conditions and trigger the adsorption process by pH adjustment. In this work, we present an alternative approach to support laser-generated metal nanoparticles by controlled precipitation onto thin graphene oxide (GO) nanosheets via a kinetically barrierless process induced by high ionic strength. This enables supporting the nanoparticles on the GO sheets with a uniform distribution even though they share a similar IEP. The broad applicability of this method is demonstrated by using different metals, nanoparticle diameters, and mass loadings. In summary, this approach allows supporting nanoparticles regardless of their surface charge.

Resolving the interactions between hydrophilic CdTe quantum dots and positively charged membranes at the nanoscale

The use of quantum dot nanoparticles (QDs) in bio-applications has gained quite some interest and requires a deep understanding of their interactions with model cell membranes. This involves assessing the extent of nanoparticle disruption of the membrane and how it depends on both nanoparticle and membrane physicochemical properties. Surface charge plays an important role in nanoparticle adsorption, which is primarily driven by electrostatic interactions; yet, once adsorbed, most reported works overlook the subsequent spatial nanoparticle insertion and location within the membrane. There is therefore a need for studies to assess the mutual role of membrane and nanoparticle charge into membrane structure and stability at the nanoscale, with a view to better design and control the functionality of these nanomaterials. In this work, we have resolved the extent of the interactions between hydrophilic, negatively charged CdTe QDs and positively charged lipid bilayers. A multiscale combination of surface-sensitive techniques enabled probing how surface charge mediates QD adsorption and membrane reorganization. Increasing membrane surface charge results into a larger adsorption of oppositely charged QDs, concomitantly inducing structural changes. Hydration of the membrane hydrophobic parts by QDs goes deeper into the inner leaflet with increasing membrane charge, resulting in supported lipid bilayers with decreased nanomechanical stability.

Encapsulation of β-carotene in Pickering emulsions stabilized by self-aggregated chitosan nanoparticles: Factors affecting β-carotene stability

For conventional emulsions used to encapsulate easily degradable bioactive compounds, achieving small droplet size and high encapsulation capacity is a challenging. Pickering emulsions stabilized by self-aggregated chitosan particles may offer high encapsulation efficiency due to the robust mechanical barrier formed by solid particles adsorbed at the oil-water interface. Therefore, the effects of pH, chitosan concentration, oil volume fraction, homogenization pressure, and homogenization cycle on the stability of chitosan Pickering emulsions and the degradation of β-carotene were investigated. Effective interfacial adsorption of chitosan nanoparticles and moderate homogenization intensity facilitated the formation of small emulsion droplets. Unlike conventional emulsions, chitosan Pickering emulsions with smaller droplets provided enhanced protection for β-carotene. This enhancement was primarily attributed to the improved interfacial coverage of chitosan nanoparticles with smaller droplet sizes, which was advantageous for β-carotene protection. The optimal conditions for preparing β-carotene-loaded chitosan Pickering emulsions were as follows: pH 6.5, chitosan concentration of 1.0 wt%, oil volume fraction of 20 %, homogenization pressure of 90 MPa, and 6 homogenization cycles. These findings indicate that chitosan Pickering emulsions are well-suited for encapsulating β-carotene with both small droplet size and high encapsulation efficiency.