Search Results (11)

The increasing demand for freshwater resources, coupled with industrial pollution, necessitates improved water treatment technologies. This study investigates the potential of quartz-based filtration systems enhanced with hydrophilic nanoparticles for efficient oil-water separation. The quartz material, abundant and cost-effective, was processed and modified through sequential coatings to enhance its hydrophilicity and separation efficiency. Comprehensive characterization techniques, including SEM, XRD, and Raman spectroscopy, were employed to evaluate surface morphology, chemical composition, and structural integrity at different stages of coating. The findings demonstrated that the first coating achieved the most uniform nanoparticle distribution, significantly improving hydrophilicity and separation efficiency, reducing oil content in filtrates to 17.3 mg/L. Subsequent coatings resulted in agglomeration and pore clogging, leading to diminished performance. Validation through mathematical models corroborated experimental observations, confirming the first coating’s superior balance of nanoparticle integration, permeability, and separation efficiency. This research highlights the potential of surface-engineered quartz as a scalable, cost-effective solution for sustainable water reuse. Future work will focus on optimizing coating techniques, scaling up, and integrating the system with complementary technologies to enhance water treatment processes. Full article

This study investigated the performance of photocatalytic titanium dioxide microfiltration membranes with an average pore size of approximately 180 nm and ultrafiltration membranes with an average pore size of around 40 nm fabricated with the suspension plasma spray process. The membranes were evaluated for their filtration performance using SiO₂ particles of different sizes and polyethylene oxide with molecular weights of 20 kDa to 1000 kDa, and the fouling parameters were characterized. The rejection rate was enhanced by increasing the thickness of the membranes. This effect was more pronounced with the ultrafiltration membranes. The rejection rate of the ultrafiltration membrane was improved significantly after filling the larger pores on the surface with agglomerates of titanium dioxide nanoparticles. The self-cleaning performance of the membranes was assessed under visible light. Both ultrafiltration and microfiltration membranes showed a flux recovery under visible light illumination due to the photocatalytic activity of titanium dioxide. The membranes also show a flux recovery of more than 90%. Full article

We developed and optimized an electrocatalytic filtration system to catalytically hydrodechlorinate chlorophenolic compounds. A key part of the system was the cathode, which consisted of a filter constructed with electroactive carbon nanotubes (CNTs) functionalized with atomically precise gold nanoclusters (AuNCs). In the functional membrane electrode, the AuNCs attached to the CNTs functioned as a highly effective hydrodechlorination catalyst. Additionally, the ligands of the AuNCs facilitated the binding of the AuNCs with the CNT and protected the Au core from agglomeration. Atomic H* was the primary reactive species in the system, but direct reduction by cathode electrons also contributed to the elimination of 2,4-dichlorophenol (2,4-DCP) by hydrodechlorination. The generated atomic H* was able to break the C–Cl bond to achieve the rapid hydrodechlorination of 2,4-DCP into phenol, with 91.5% 2,4-DCP removal within 120 min. The AuNC catalysts attached to the CNT exceeded the best catalytic activity of larger nanoparticles (e.g., AuNPs), while the flow-through construction performed better than a standard batch reactor due to the convection-enhanced mass transport. The study provides an environmentally friendly strategy for the elimination of pervasive halogenated organic contaminants using a highly efficient, stable and recyclable system for hydrodechlorination that integrates nanofiltration and electrochemistry. Full article

This paper presents an analysis of the fouling of a ceramic membrane by a mixture containing high concentrations of humic acid and colloidal silica during cross-flow ultrafiltration under various operating conditions. Two types of feed water were tested: feed water containing humic acid and feed water containing a mixture of humic acid and colloidal silica. The colloidal silica exacerbated the fouling, yielding lower fluxes (109–394 L m⁻² h⁻¹) compared to the humic acid feed water (205–850 L m⁻² h⁻¹), while the retentions were higher except for the highest cross-flow rate. For the humic acid feed water, the irreversible resistance prevails under the cross-flow rate of 5 L min⁻¹. During the filtration of an organic–inorganic mixture, the reversible resistance due to the formation of a colloidal cake layer prevails under all operating conditions with an exception. The exception is the filtration of the organic–inorganic mixture of a 50 mg L⁻¹ humic acid concentration which resulted in a lower flux than the one of a 150 mg L⁻¹ humic acid concentration under 150 kPa and a cross-flow rate of 5 L min⁻¹. Here, the irreversible fouling is unexpectedly overcome. This is unusual and occurs due to the low agglomeration at low concentrations of humic acid under a high cross-flow rate. Under lower transmembrane pressure and a moderate cross-flow rate, fouling can be mitigated, and relatively high fluxes are yielded with high retentions even in the presence of nanoparticles. In this way, colloidal silica influences the minimization of membrane fouling by organic humic acid contributing to the control of in-pore organic fouling. Full article

Background: Cyanobacteria are considered as green nano-factories. Manipulation of the size of biogenic silver nanoparticles is needed to produce particles that suit the different applications such as the use as antibacterial agents. The present study attempts to manipulate the size of biosynthesized silver nanoparticles produced by cyanobacteria and to test the different-sized nanoparticles against pathogenic clinical bacteria. Methods: Cyanothece-like. coccoid unicellular cyanobacterium was tested for its ability to biosynthesize nanosilver particles of different sizes. A stock solution of silver nitrate was prepared from which three different concentrations were added to cyanobacterial culture. UV-visible spectroscopy and FTIR were conducted to characterize the silver nanoparticles produced in the cell free filtrate. Dynamic Light Scattering (DLS) was performed to determine the size of the nanoparticles produced at each concentration. The antimicrobial bioassays were conducted on broad host methicillin-resistant Staphylococcus aureus (MRSA), and Streptococcus sp., was conducted to detect the nanoparticle size that was most efficient as an antimicrobial agent. Results. The UV-Visible spectra showed excellent congruence of the plasmon peak characteristic of nanosilver at 450 nm for all three different concentrations, varying peak heights were recorded according to the concentration used. The FTIR of the three solutions revealed the absence of characteristic functional groups in the solution. All three concentrations showed spectra at 1636 and 2050–2290 nm indicating uniformity of composition. Moreover, DLS analysis revealed that the silver nanoparticles produced with lowest concentration of precursor AgNO₃ had smallest size followed by those resulting from the higher precursor concentration. The nanoparticles resulting from highest concentration of precursor AgNO₃ were the biggest in size and tending to agglomerate when their size was above 100 nm. The three types of differently-sized silver nanoparticles were used against two bacterial pathogenic strains with broad host range; MRSA-(Methicillin-resistant Staphylococcus aureus) and Streptococcus sp. The three types of nanoparticles showed antimicrobial effects with the smallest nanoparticles being the most efficient in inhibiting bacterial growth. Discussion: Nanosilver particles biosynthesized by Cyanothece-like cyanobacterium can serve as antibacterial agent against pathogens including multi-drug resistant strains. The most appropriate nanoparticle size for efficient antimicrobial activity had to be identified. Hence, size-manipulation experiment was conducted to find the most effective size of nanosilver particles. This size manipulation was achieved by controlling the amount of starting precursor. Excessive precursor material resulted in the agglomeration of the silver nanoparticles to a size greater than 100 nm. Thereby decreasing their ability to penetrate into the inner vicinity of microbial cells and consequently decreasing their antibacterial potency. Conclusion: Antibacterial nanosilver particles can be biosynthesized and their size manipulated by green synthesis. The use of biogenic nanosilver particles as small as possible is recommended to obtain effective antibacterial agents. Full article

The study investigated the phenomenon of the fast aggregation of single-domain magnetic iron oxide nanoparticles in stable aqueous colloidal suspensions due to the presence of a radio-frequency (RF) magnetic field. Single-domain nanoparticles have specific magnetic properties, especially the unique property of absorbing the energy of such a field and releasing it in the form of heat. The localized heating causes the colloid to become unstable, leading to faster agglomeration of nanoparticles and, consequently, to rapid sedimentation. It has been shown that the destabilization of a stable magnetic nanoparticle colloid by the RF magnetic field can be used for the controlled filtration of larger agglomerates of the colloid solution. Two particular cases of stable colloidal suspensions were considered: a suspension of the bare nanoparticles in an alkaline solution and the silica-stabilized nanoparticles in a neutral solution. The obtained results are important primarily for biomedical applications and wastewater treatment. Full article

Among the various methods for the preparation of nanoparticles, a sparking process at atmospheric pressure is of interest because it is a simple method for producing nanoparticles ranging from a few nanometer-sized particles to agglomerated film structures. In this research, we studied the effects of metal electrode properties on nanoparticle sizes. The experiments were carried out by applying a high voltage to different metal sparkling tips. The transfer of energies from positive ions and electron bombardments induced the melting and vaporization of electrode metals. Based on this research, we have developed a model to describe the formation of a nanoparticle film on the substrate, placed under the sparking gap, and the nanostructure produced by metal vapor on the sparking electrodes. The model provides a realistic tool that can be used for the design of a large-scale coating and the application of nanoparticles developed by this process for the filtration of PM2.5 mask fabric by air. Full article

This study focused on developing a hydrophilic hybrid polyvinylidene fluoride (PVDF)-polyethylene glycol (PEG) hollow membrane by incorporating Nano-magnesium oxide (NMO) as a potent antifouling mediator. The Nano-hybrid hollow fibers with varied loading of NMO (0 g; 0.25 g; 0.50 g; 0.75 g and 1.25 g) were spun through phase inversion technique. The resultants Nano-hybrid fibers were characterized and compared based on SEM, EDX, contact angle, surface zeta-potential, permeability flux, fouling resistance and color rejection from palm oil mill effluent (POME). Noticeably, the permeability flux, fouling resistance and color rejection improved with the increase in NMO loading. PVDF-PEG with 0.50 g-NMO loading displayed an outstanding performance with 198.35 L/m²·h, 61.33 L/m²·h and 74.65% of water flux, POME flux and color rejection from POME, respectively. More so, a remarkable fouling resistance were obtained such that the flux recovery, reversible fouling percentage and irreversible fouling percentage remains relatively steady at 90.98%, 61.39% and 7.68%, respectively, even after 3 cycles of continuous filtrations for a total period of 9 h. However, at excess loading of 0.75 and 1.25 g-NMO, deterioration in the flux and fouling resistance was observed. This was due to the agglomeration of nanoparticles within the matrix structure at the excessive loading. Full article

Molecular scale modifications were achieved by spontaneous polarization which is favored in enhancements of β-crystallization phase inside polyvinylidene fluoride (PVDF) nanofibers (NFs). These improvements were much more effective in nano and submicron fibers compared to fibers with relatively larger diameters. Metallic nanoparticles (NPs) supported by nanofibrous membranes opened new vistas in filtration, catalysis, and serving as most reliable resources in numerous other industrial applications. In this research, hydrogenation of phenol was studied as a model to test the effectiveness of polarized PVDF nanofiber support embedded with agglomerated palladium (Pd) metallic nanoparticle diameters ranging from 5–50 nm supported on polymeric PVDF NFs with ~200 nm in cross-sectional diameters. Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), Atomic Force Microscopy (AFM), Energy Dispersive X-Ray Spectroscopy (EDX), Fourier Transform Infrared Spectroscopy (FTIR) and other analytical analysis revealed both molecular and surface morphological changes associated with polarization treatment. The results showed that the fibers mats heated to their curie temperature (150 °C) increased the catalytic activity and decreased the selectivity by yielding substantial amounts of undesired product (cyclohexanol) alongside with the desired product (cyclohexanone). Over 95% phenol conversion with excellent cyclohexanone selectivity was obtained less than nine hours of reaction using the polarized PVDF nanofibers as catalytic support structures. Full article

In this study, the antifouling properties of polyethersulfone (PES) membranes blended with different amounts of ZnO nanoparticles and a fixed ratio of N-methyl-2-pyrrolidone (NMP)-acetone mixture as a solvent were investigated. The properties and performance of the fabricated membranes were examined in terms of hydrophilicity, porosity, pore size, surface and cross-section image using scanning electron microscopy (SEM), surface roughness using atomic force microscopy (AFM), pure water flux, and humic acid filtration. Addition of ZnO as expected was found to improve the hydrophilicity as well as to encourage pore formation. However, the agglomeration of ZnO at a higher concentration cannot be avoided even when dissolved in a mixed solvent. The presence of highly volatile acetone contributed to the tight skin layer of the membrane which shows remarkable antifouling ability with the highest flux recovery ratio and negligible irreversible fouling. ZnO NPs in acetone/NMP mixed solvent shows an improvement in flux and rejection, but, the fouling resistance was moderate compared to the pristine membrane. Full article

Polyvinylidene difluoride (PVDF) mixed matrix membranes loaded with inorganic TiO₂ nanoparticles have received increasing attention in the last few years as self-cleaning membranes for possible application in wastewater treatment and seawater filtration. These novel membranes show increased hydrophilicity, stability and catalytic activity under UV-A irradiation. In this work, PVDF-TiO₂ hollow fibers were prepared by employing new strategies for enhancing the stability of the TiO₂ dispersion, reducing particle agglomeration and improving their distribution. The spinning conditions for producing ultrafiltration hollow fiber membranes from PVDF material and nano-TiO₂ were investigated. Finally, the optimized fibers have been characterized and tested for methylene blue (MB) degradation in water and salty seawater, revealing good permeability, long-term stability under UV-A irradiation, and photo-catalytic activity in both test solutions. Full article