Hydrophilic Nanoparticles Research Articles

Effect of Janus nanoparticles on foam snap off in porous media

Abstract Nanoparticles can be adsorbed at the gas-liquid interface to improve the stability of foam. However, homogeneous nanoparticles exhibit low surface activity, and their migration to the gas-liquid interface requires significant energy input. This leads to harsh foaming conditions and severely limits the application of homogeneous nanoparticles in foam stability. A microfluidic visualisation model for the study of Janus nanoparticle complex systems was used to investigate the formation behaviour of trapped bubbles in a single connected pore-throat model. The foam generated in the pore showed reduced quantities, sizes, improved quality, and enhanced stability compared to both surfactant systems and hydrophilic nanoparticle complex systems.

Vibration-triggered spreading of nanofluid drops

This study explores the effects of nanoparticles on the dynamics of drop spreading under external vibration, presenting an advance in the understanding of nanofluid behavior on vibrating substrates. This work introduces insights into nanoparticle-mediated drop spreading, offering implications for improving particulate coatings, mini-mixers, and particle segregation technologies. By employing a twofold approach that combines oscillating drop dynamics with internal flow pattern analysis, we find how even small concentrations of hydrophilic or hydrophobized silica nanoparticles inside water sessile droplets significantly alter the spreading process on silanized glass surfaces. Our study allows distinct drop spreading regimes to be identified based on nanoparticle concentration and vibration amplitude, for both hydrophilic and hydrophobized nanoparticles. Through a comprehensive analysis, we demonstrate that the vibration-triggered spreading of nanofluids can lead to a stable and controlled manipulation of complex liquids.

PH-Controllable Redox Responsive Amphiphilic Viologens for Switchable Emulsions.

A pH and redox dual responsive amphiphilic viologen is synthesized, which can be reversibly transformed among the zwitterionic (SVa), monovalent anionic (SV+), and divalent anionic (SVH2+) forms upon pH variation, exhibiting pH-controllable redox responsive properties. Switchable Pickering emulsions with different droplet size and viscosity are prepared by the mixture of hydrophilic silica nanoparticles and the viologens (SV+ or SVH2+) at acidic conditions, while such combination yielded an oil-in-dispersion emulsion at neutral pH value. Not only can rapid reversible demulsification/stabilization of the Pickering emulsions be achieved by redox reactions, but the rate of redox-demulsification can also be controlled by pH trigger. The dual-responsive amphiphilic viologens have potential applications in developing intelligent colloid materials and molecular logic systems.

Mussel-inspired fabrication of fouling-resistant PPSU-based nanocomposite membrane using polydopamine and tannic acid-functionalized CeO2 nanoparticles towards effective oil-water emulsions separation

Surface modification of membranes using hydrophilic nanoparticles has proved promising to improve the surface wettability and antifouling properties of the membranes that are otherwise prone to the attachment of oil droplets. Nonetheless, the strong adhesion of nanoparticles onto the membrane surface and their long-term performance pose problems for their widespread application. To address these issues, a novel organic-inorganic hybrid coating was constructed onto surfaces of polyphenylsulfone (PPSU) ultrafiltration membrane via simultaneous deposition of mussel-inspired polydopamine (PDA) followed by immobilization of tannic-acid functionalized cerium oxide (CeO2) nanoparticles. These prepared membranes were characterized by FTIR, XPS, FESEM, EDX, pore size, water contact angle (WCA), underwater oil contact angle (UOCA), and separation performance. The effects of functionalization and nanoparticle concentration on membrane properties were investigated. SEM and EDX results showed that functionalized nanoparticles (up to optimum concentration: 0.05 wt%) were uniformly distributed onto the membrane surface, which exhibited increase in permeate flux (∼375 %), UOCA (∼36 %), Fouling resistance ratio (FRR ∼ 300 %) with a decrease in irreversible fouling (∼94 %) and WCA (∼80 %) and high oil rejection of > 99 % compared to pristine PPSU membrane. Long-term operation (for six cycles) indicates that the optimum membrane possessed high efficiency and durability for oil-in-water emulsion separation due to superb antifouling properties and strong binding of the functionalized nanoparticles onto the membrane surface.

Dispersion and Dosimetric Challenges of Hydrophobic Carbon-Based Nanoparticles in In Vitro Cellular Studies.

Methodologies across the dispersion preparation, characterization, and cellular dosimetry of hydrophilic nanoparticles (NPs) have been developed and used extensively in the field of nanotoxicology. However, hydrophobic NPs pose a challenge for dispersion in aqueous culture media using conventional methods that include sonication followed by mixing in the culture medium of interest and cellular dosimetry. In this study, a robust methodology for the preparation of stable dispersions of hydrophobic NPs for cellular studies is developed by introducing continuous energy over time via stirring in the culture medium followed by dispersion characterization and cellular dosimetry. The stirring energy and the presence of proteins in the culture medium result in the formation of a protein corona around the NPs, stabilizing their dispersion, which can be used for in vitro cellular studies. The identification of the optimal stirring time is crucial for achieving dispersion and stability. This is assessed through a comprehensive stability testing protocol employing dynamic light scattering to evaluate the particle size distribution stability and polydispersity. Additionally, the effective density of the NPs is obtained for the stable NP dispersions using the volumetric centrifugation method, while cellular dosimetry calculations are done using available cellular computational modeling, mirroring approaches used for hydrophilic NPs. The robustness of the proposed dispersion approach is showcased using a highly hydrophobic NP model (black carbon NPs) and two culture media, RPMI medium and SABM, that are widely used in cellular studies. The proposed approach for the dispersion of hydrophobic NPs results in stable dispersions in both culture media used here. The NP effective density of 1.03-1.07 g/cm3 measured here for black carbon NPs is close to the culture media density, resulting in slow deposition on the cells over time. So, the present methodology for dispersion and dosimetry of hydrophobic NPs is essential for the design of dose-response studies and overcoming the challenges imposed by slow particle deposition.

Synthesis and characterization of enhanced polysulfone-based mixed matrix membranes containing ZSM-5 zeolite for protein and dye removal

In this paper, polysulfone (PSf)-based ultrafiltration (UF) mixed matrix membranes (MMMs) embedded with ZSM-5 zeolite nanoparticles were synthesized via the NIPS method. The membranes were characterized by FESEM, ATR-FTIR, AFM, and tensile analyses, along with contact angle, porosity, and mean pore size measurements. The FESEM images indicated that the addition of hydrophilic ZSM-5 nanoparticles has led to formation of more and larger finger-like macrovoids. Moreover, hydrophilicity and pure water flux (PWF) values were consequently augmented, which was also approved by water contact angle reduction. The maximum PWF was equal to 394.7 L m-2h−1 at 3 bar for the optimum MMM, containing 1 wt% ZSM-5 which is 125.4 % greater than the value for the bare membrane. In addition, filtration of the bovine serum albumin (BSA) protein and aqueous solutions of two organic dyes were carried out. The highest BSA flux value was obtained 217.9 L m-2h−1 for the optimum membrane, where the BSA rejection values were all greater than 98 %. Furthermore, the optimum MMM displayed the highest flux recovery ratio (FRR%) of 60.1 % as well as the dyes rejection values equal to 95.5 % and 74.1 % for reactive black 5 (RB 5) and reactive yellow 160 (RY 160), respectively, representing its great potential to be applied in various wastewater treatment applications.

Effects of Nanoparticle Wettability on the Meniscus Stability of Oil-Water Systems: A Coarse-Grained Modeling Approach.

A coarse-grained modeling approach is employed to probe the effect of nanoparticles and their wettability on the stability of the interface between two immiscible fluids. In this study, pure oil (dodecane) and water are placed side by side in a nanochannel, forming a meniscus. Homogeneous hydrophilic nanoparticles, Janus particles, and homogeneous hydrophobic nanoparticles are placed at the oil-water interface, and their dynamics are studied as they rearrange at the oil-water interface. The results show that when the water is set in motion, two instabilities occur: the formation of fingers and the detachment of water from the channel wall. It is observed that the formation of fingers is affected by the wettability of the nanoparticles. The second instability may lead to the formation of a drop that propagates through the channel. However, it is found that the wetting properties of the nanoparticles do not affect the critical flow rate for the detachment of the water from the wall. Therefore, detachment occurs at the same three-phase contact angle regardless of the nanoparticle wetting properties. These findings can be important for industrial applications such as enhanced oil recovery, separation technologies, and microfluidic and nanofluidic technologies.

Impact of cationic surfactant-coated hydrophilic nanoparticles on polymeric solution performance in chemical enhanced oil recovery (CEOR) from a two-dimensional porous medium

This study aims to investigate the mechanisms underlying enhanced oil recovery (EOR) through chemical injection and explore the key parameters influencing these mechanisms in a two-dimensional porous medium. Distilled water, polyacrylamide (PAM), α-Al2O3 nanoparticles, and cetyltrimethylammonium bromide (CTAB) surfactant were employed for this purpose. The effects of interfacial tension (IFT), viscosity, and zeta potential measurement were also examined. The results revealed that the injection of PAM polymer increased the viscosity of the displacing fluid, and enhanced the sweep efficiency. This resulted in a 35 % increase in the oil recovery factor compared to the water injection alone. Furthermore, the introduction of alumina (α-Al2O3) nanoparticles altered the wettability and stabilized the emulsion, leading to a further increase in the oil recovery factor. In the optimal state, the oil recovery factor reached 63.2 %. Moreover, the study of various concentrations of polymer and nanoparticles illustrated that low concentrations of polymer and high concentrations of nanoparticles in the base fluid resulted in higher oil recovery factors. Furthermore, adding CTAB surfactant ended a significant reduction in IFT, with a decrease from 45.03 to 10.33 mN/m. This reduction resulted in the highest oil recovery factor of 69 %. Consequently, the highest oil recovery factor was achieved using PAM polymer at a concentration of 500 ppm, α-Al2O3 nanoparticles at a concentration of 0.1 wt%, and CTAB surfactant at a critical micelle concentration of 1 mM in the base fluid (pure water), with a constant injection flowrate of 0.1 ml/min.

Design of an ultra-sensitive nanoprobe based on poly β-cyclodextrin for formaldehyde detection in food and biological samples

Formaldehyde is widely used in daily life and can be generated endogenously through diverse biological processes. However, formaldehyde may cause severe threat to the health of humanity. In this work, we designed a novel nanoprobe NaP@Pβ-CD through the host-guest self-assembly between poly β-cyclodextrins (Pβ-CD) and naphthalimide (NaP). The NaP is enclosed in the Pβ-CD cavity, forming hydrophilic nanoparticles. Formaldehyde can trigger “on” fluorescence response of NaP fluorophore and the detection can be carried out in aqueous solution. This probe has low detection limit (16.8 nM), a fast response to FA (5 min), high selectivity, good biocompatibility and excellent stability. More importantly, it shows excellent sensing capability totally in water without requiring any organic solvent. Therefore, the NaP@Pβ-CD could be successfully applied to formaldehyde detection in food, living cells, and organisms in vivo.

Nanofluid Drop Impact on Heated Surfaces.

We experimentally elucidate the impact dynamics of ethylene glycol (EG) droplets laden with both hydrophilic and hydrophobic SiO2 nanoparticles (NPs) onto a flat heated surface in non-boiling, boiling, and Leidenfrost regimes. We use seven nanofluid concentrations (Cp), ranging from 0.89 to 64.3 wt %, and control the surface temperature (Ts) between 100 and 400 °C, while the nanofluid droplet's impact velocity is constant at 0.22 ± 0.02 m/s. Phase diagrams of impact outcomes are established to illustrate the effect of the additive nanoparticles on the droplets' impact dynamics, revealing that nanoparticles modify droplet impact behaviors differently in each regime. In the non-boiling regime, the droplet spreading profile remains unaffected by nanoparticles up to Cp < 11.9 wt % before reaching the maximum spreading diameter (βmax). For nanofluid drops with higher nanofluid concentration, the increasing viscosity with concentration is likely to be the primary factor that affects the droplets' spreading profile in the non-boiling regime Ts ≲ Tsat ≈ 200 °C, as the saturation temperature. In the boiling regime 200 °C < Ts ≲ 350 °C, a small amount of nanoparticle addition (Cp = 0.89 wt %) promotes atomization regardless of nanoparticle wettability. Finally, manifested in a complete rebound due to an intervening vapor layer, the Leidenfrost temperature (TL) of the nanofluid droplets is affected by both nanofluid concentration and nanoparticles' wettability. The nanofluid droplets' TL increases with higher nanofluid concentration; moreover, this Leidenfrost temperature increment is more significant for EG droplets laden with hydrophobic nanoparticles. Our results quantitatively reveal the significant influence of nanoparticle concentrations and wettability on drop spreading, impact outcome, and Leidenfrost temperature on heat surfaces, potentially benefiting applications in coating, spraying, and cooling.

Hydrophilic Biocompatible Fluorescent Organic Nanoparticles as Nanocarriers for Biosourced Photosensitizers for Photodynamic Therapy.

Most photosensitizers of interest for photodynamic therapy-especially porphyrinoids and chlorins-are hydrophobic. To circumvent this difficulty, the use of nanocarriers is an attractive strategy. In this perspective, we have developed highly water-soluble and biocompatible fluorescent organic nanoparticles (FONPs) made from citric acid and diethyltriamine which are then activated by ethlynene diamine as nanoplatforms for efficient photosensitizers (PSs). Purpurin 18 (Pp18) was selected as a biosourced chlorin photosensitizer combining the efficient single oxygen generation ability and suitable absorption in the biological spectral window. The simple reaction of activated FONPs with Pp18, which contains a reactive anhydride ring, yielded nanoparticles containing both Pp18 and Cp6 derivatives. These functionalized nanoparticles combine solubility in water, high singlet oxygen generation quantum yield in aqueous media (0.72) and absorption both in the near UV region (FONPS) and in the visible region (Soret band approximately 420 nm as well as Q bands at 500 nm, 560 nm, 660 nm and 710 nm). The functionalized nanoparticles retain the blue fluorescence of FONPs when excited in the near UV region but also show deep-red or NIR fluorescence when excited in the visible absorption bands of the PSs (typically at 520 nm, 660 nm or 710 nm). Moreover, these nanoparticles behave as efficient photosensitizers inducing colorectal cancer cell (HCT116 and HT-29 cell lines) death upon illumination at 650 nm. Half maximal inhibitory concentration (IC50) values down to, respectively, 0.04 and 0.13 nmol/mL were observed showing the potential of FONPs[Cp6] for the PDT treatment of cancer. In conclusion, we have shown that these novel biocompatible nanoparticles, which can be elaborated from biosourced components, both show deep-red emission upon excitation in the red region and are able to produce singlet oxygen with high efficiency in aqueous environments. Moreover, they show high PDT efficiency on colorectal cancer cells upon excitation in the deep red region. As such, these functional organic nanoparticles hold promise both for PDT treatment and theranostics.

Silk‐Based Functional Inks with Color‐Tunable Light Upconversion for Printing on Arbitrary Surfaces

AbstractA biocompatible and versatile silk‐based functional ink with hydrophilic upconversion nanoparticles (UCNPs) that can be printed or painted on arbitrary substrates, including biological surfaces is demonstrated. Hydrophilic UCNPs, ready to be dispersed in aqueous silk fibroin solution, are synthesized in large quantities via facile hydrothermal synthesis using citric acid. Based on a systematic study of dopant control to achieve robust red emission from citrate‐capped UCNPs, three primary colors are obtained, which serve as the basis for the expansion of the color palette. The synthesized UCNPs are homogeneously dispersed in regenerated silk fibroin solutions derived from Bombyx mori cocoons to produce water‐based functional inks. Cyan, magenta, and yellow (CMY) inks are created by combining red, green, and blue (RGB) inks. Demonstrator devices, where a variety of colorful patterns and codes are revealed only under near‐infrared irradiation, are realized through stencil printing or brush painting on flexible polymer films, fruit, leaves, silkworm cocoons, and pig skin. The patterns and codes are highly heat resistant (≈230 °C) and can be easily washed off with water after use. The printable/paintable inks and functions proposed here will provide new opportunities for applications where sustainability, biocompatibility, and intentional luminescence are simultaneously required.

Berberine-loaded polylactic acid nanofiber scaffold as a drug delivery system: The relationship between chemical characteristics, drug-release behavior, and antibacterial efficiency.

Hydrophobic berberine powder (BBR) and hydrophilic BBR nanoparticles (BBR NPs) were loaded into an electrospun polylactic acid (PLA) nanofiber scaffold for modulating the release behavior of BBR in an aqueous medium. The BBR release from the BBR/PLA and BBR NPs/PLA nanofiber scaffolds was investigated in relation to their chemical characteristics, BBR dispersion into nanofibers, and wettability. The BBR release profiles strongly influenced the antibacterial efficiency of the scaffolds over time. When the BBR was loaded, the BBR/PLA nanofiber scaffold exhibited an extremely hydrophobic feature, causing a triphasic release profile in which only 9.8 wt % of the loaded BBR was released in the first 24 h. This resulted in a negligible inhibitory effect against methicillin-resistant Staphylococcus aureus bacteria. Meanwhile, the BBR NPs/PLA nanofiber scaffold had more wettability and higher concentration of BBR NPs dispersed on the surface of PLA nanofibers. This led to a sustained release of 75 wt % of the loaded BBR during the first 24 h, and consequently boosted the antibacterial effectiveness. Moreover, the cytotoxicity test revealed that the BBR NPs/PLA nanofiber scaffold did not induce any changes in morphology and proliferation of MA-104 cell monolayers. It suggests that the BBR/PLA and BBR NPs/PLA nanofiber scaffolds can be used in different biomedical applications, such as wound dressing, drug delivery systems, and tissue engineering, according to the requirement of BBR concentration for the desired therapeutic effects.

Enhancing natural gas dehumidification with Pebax/Silica mixed matrix membrane: a comprehensive study

ABSTRACT In this study, a new polymer membrane was developed for natural gas dehumidification using the combination of hydrophilic silica nanoparticles in the Pebax polymer matrix. The membranes were characterized using various analytical methods including FTIR, XRD, SEM, and TGA. The results indicated that adding nanoparticles increased the porosity and thermal stability of the membranes. Also, the enhancement of copolymer hydrophilicity was confirmed by reducing contact angles. The study found that increasing the nanoparticle content from 0 w% to 3 w% at 15 bar pressure resulted in a 33% increase in water permeability and a 12% increase in methane permeability. Adding of silica also increased the H2O/CH4 selectivity from 24.17 to 27.34. Moreover, at higher temperatures (from 25 to 55°C), the permeability of H2O and CH4 reached 171.3 and 10.71 bar, respectively. The findings of this study show that the inclusion of hydrophilic silica nanoparticles in the Pebax matrix can enhance the efficiency of membranes for natural gas dehumidification. Additionally, the study highlights the significance of temperature in the design and implementation of such membranes.

Experimental and analytical studies on latent heat of hydrated salt/modified EG-based form-stable composite PCMs for energy storage application

Expanded graphite (EG) is often used to encase phase change materials (PCMs) and improve their thermal performance. However, EG's effectiveness when used with disodium hydrogen phosphate dodecahydrate (DHPD) as a hydrated salt is diminished, due to its hydrophobic property. This study proposes modifying the hydrophobic surface of EG with highly hydrophilic nanoparticles, such as SiO2 and TiO2, to address this shortcoming and boost its hydrophilicity. Herein, the nanoparticles were synthesized by the sol-gel technique and mixed with EG to construct a modified EG (MEG). The microstructure, morphology, and adsorption ability of MEG were analyzed. Additionally, the thermal properties, as well as the thermal stability of form-stable composite PCMs, were investigated. The results revealed that by varying the mass ratio of SiO2@TiO2 in MEG, the supercooling degree of the form-stable composite PCMs decreased by 77.36%–78.49%. With 9% SiO2@TiO2 in MEG, the water contact angle of MEG was optimal, and the form-stable composite PCMs prepared (DSMEG3) exhibited a phase change temperature and latent heat of 32.88 °C and 142.13 J/g, respectively. This experimental latent heat was slightly lower than the calculated latent heat by 0.12 J/g. Meanwhile, the supercooling degree decreased to 3.01 °C, and the thermal conductivity increased to 1.23 W/(m ∙ K), which was 1.73 times than that of DHPD. Moreover, DSMEG3 also showed good shape stability, preventing leakage. Therefore, the form-stable composite PCMs, as prepared, are a great potential candidate for the energy storage applications.

Improved properties and salt rejection of polysulfone membrane by incorporation of hydrophilic cobalt-doped ZnO nanoparticles

In this study, the nanoparticles (NPs) of ZnO and Co2+ ions doped ZnO (doped ZnO) were incorporated into a matrix of polysulfone (PSf) membranes to enhance their surface properties prepared using a simple wet phase inversion technique. The hybrid PSf membranes were fabricated with 0.5 wt. % of ZnO and doped ZnO NPs. These membranes were characterized using XRD, TGA, FESEM-EDX, and salt rejection performance. The hydrophilicity of PSf membranes was improved by adding of ZnO and doped ZnO NPs which showed a decrease in contact angle values from 82° to 62° with an increased flux with water. Among the prepared membranes, doped ZnO NPs showed the highest salt rejection for both sodium chloride (NaCl) and sodium sulfate (Na2SO4) compared to pure PSf and PSf with ZnO NPs which confirm the improvement contact angle and water permeability. Overall, the results of this study showed that embedding a small amount of Co2+ ions doped ZnO NPs with PSf has significant potential to be applied in industrial-scale membrane applications.

Tailoring morphology for improved dispersibility of hydrophilic silica nanoparticles to fabricate thin-film nanocomposite membranes

Improving the dispersibility of nanomaterials is a promising approach to enhance the performance of thin-film nanocomposite (TFN) membranes. In this study, hydrophilic nonporous, mesoporous, and dendritic mesoporous silica nanoparticles (NSNs, MSNs, and DMSNs) with a uniform particle size were utilized as aqueous phase additives to prepare TFN membranes through in-situ polymerization. The electrostatic adsorption of nanoparticles increased the concentration of amine monomers on the surface of the polysulfone (PSF) substrate. In collaboration with the steric hindrance effect, nanoparticles restricted the diffusion of piperazine (PIP) into the organic phase to polymerize with the acyl chloride monomers. Compared to TFC-0, the TFN membranes exhibited a rougher surface with increased negative charge and had more channels that facilitated the transportation of water molecules. Among the nanoparticles, DMSNs exhibited excellent dispersibility, ensuring their uniform distribution within the polyamide (PA) matrix. Furthermore, DMSNs possessed an open central-radial pore structure, offering more efficient channels for water molecules to cross the membrane. Therefore, a highly crosslinked, defect-free, and hydrophilic PA layer of TFN-DMSNs was achieved. In the performance characterization, TFN-DMSNs demonstrated a high water/salt permselectivity (A/B) of up to 32.25 bar−1, and exhibited good resistance to acidic/alkaline environments as well as foulants during the operation. This study proposes a novel approach to prepare advanced TFN membranes by optimizing the morphological structure of nanoparticles.

A reflection on ‘Protein coronas suppress the hemolytic activity of hydrophilic and hydrophobic nanoparticles’

Rotello et al. reflect on their first Materials Horizons paper (Mater. Horiz., 2014, https://doi.org/10.1039/C3MH00075C) published in the inaugural issue of the journal, and discuss how their work may have influenced the research field over the past decade.

Low-cost one-pot synthesis of hydrophobic and hydrophilic monodispersed iron oxide nanoparticles

A one-pot synthesis of monodispersed iron oxide nanoparticles starting with iron nitrate and control of morphology, dimension and dispersibility.

Optimum content of incorporated nanomaterials: Characterizations and performance of mixed matrix membranes a review

Environmental concerns about chemical and biological pollution of water are of alarming proportions. Therefore, various polymeric membranes with improved mechanical and physico-chemical qualities for water treatment were developed using mixed matrix membranes (MMMs) or nanoparticles (NPs) embedded with the membranes. However, the problem of fouling and consequent higher operating and membrane replacement costs are barriers to the use of membrane technology. Therefore, a deeper comprehension of membrane fouling is not only essential for finding solutions but also a crucial factor in the development of membrane technology. The conventional blending modification would result in a large number of nanoparticles in the polymer matrix. In reality, the aggregation of nanoparticles in composite membranes is a considerable issue and would result in unfavorable changes to the features of the membrane (e.g. decreased water flux, weakened mechanical strength). In this review, it was looked into the effect of an optimal concentration of the hydrophilic nanoparticle additions to avoid the aggregation of nanoparticles in composite membranes and the reduced of using high amounts of valuable and costly nanoparticles in the membranes production and to obtain better results. The influence of the additives, such as (carbon nanotubes (CNTs), silica (SiO2), titanium dioxide (TiO2), zinc oxide (ZnO), aluminum oxide (Al2O3), and graphene oxide (GO), etc.) was investigated.