Water Purification Research Articles

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

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

Cleaning Up Metal Contamination after Decades of Energy Production and Manufacturing: Reviewing the Value in Use of Biochars for a Sustainable Future

The lasting impact of ancestral energy production operations and global manufacturing has not only generated substantial CO2 emissions, but it has also led to the release of metal-based pollutants into Earth’s water bodies. As we continue to engineer, mine (coal and metals), and now bore into geothermal wells/fracking sites for alternative energy sources, we continue to contaminate drinking water supplies with heavy metals through infiltration and diffusion, limiting progress towards achieving Sustainable Development Goals 3 (Sustainable Development Goal 3: Good health and well-being), 6 (Sustainable Development Goal 6: Clean water and sanitation), 14 (Sustainable Development Goal 14: Life below water), and 15 (Sustainable Development Goal 15: Life on land). This review shows how the research community has designed and developed mesoporous biochars with customizable pore systems, as well as functionalized biochars, to extract various heavy metals from water sources. This article investigates how biochar materials (non-activated, activated, functionalized, or hybrid structures) can be adapted to suit their purpose, highlighting their recyclability/regeneration and performance when remediating metal-based pollution in place of conventional activated carbons. By utilizing the wider circular economy, “waste-derived” carbonaceous materials will play a pivotal role in water purification for both the developed/developing world, where mining and heavy manufacturing generate the most substantial contribution to water pollution. This review encompasses a wide range of global activities that generate increased heavy metal contamination to water supplies, as well as elucidates emerging technologies that can augment environmental remediation activities, improving the quality of life and standard of living for all.

Activated carbons prepared from stump wood of various tree species by chemical activation and their application for water purification

AbstractActivated carbons (ACs) were produced from stump wood of different tree species, such as pine, bearded birch, and American black cherry using chemical activation with KOH and NaOH. The activated carbons were characterized and evaluated as adsorbents for eliminating bisphenol A (BPA) from aqueous solutions. The kinetics of adsorption and equilibrium adsorption, as well as the impact of solution pH and ionic strength, were examined. The kinetics were analyzed using the pseudo-first-order, pseudo-second-order, intra-particle diffusion, and Boyd kinetic models. The findings suggest that the adsorption kinetics followed the pseudo-second-order model. Additionally, the film diffusion was found to be the rate-determining step for the adsorption of BPA on all of the activated carbons. The data for adsorption equilibrium were tested using the Langmuir, Freundlich, and Sips equations, with results indicating that the Langmuir model was the most applicable. The capacity of activated carbons to adsorb BPA was dependent on their surface area. Higher BET surface areas resulted in increased adsorption. The birch-derived AC activated by NaOH had a monolayer adsorption capacity of 1.980 mmol/g, while the AC from black cherry activated with KOH had 2.195 mmol/g. The adsorption of BPA was pH-dependent, and no effect of ionic strength was observed. The activated carbons had very high adsorption capacities, indicating that stump wood is an excellent precursor for the production of highly effective adsorbents.

Safety and security of household water purifiers against pathogenic microbial contamination and bio-risk evaluation of their microbial community structures

Household water filters, particularly point-of-use systems, are crucial to ensure safe drinking water consumption by eliminating microbial contaminants. This study evaluated the efficacy of three types of water purifiers (ultrafiltration [UF], nanofiltration [NF], and reverse osmosis [RO]) against microbial contamination. In our experiments, Escherichia coli and bacteriophage MS2 were used as two microbial indicators in daily household settings to track the spatial and temporal profiles of their behavior from the filter inlets to in-UF, NF, and RO water purifiers, and then to effluents. The results showed that both NF and RO water purifiers removed 100 % of the indicator organisms. The UF water purifier achieved 100 % removal of E. coli, but the removal of MS2 phage was poor. The presence of coexisting ions and natural organic matter in tap water can significantly affect the behavior of MS2 phages during the water treatment process. Their presence reduces the charge repulsion effect of the UF membrane on the MS2 phage as well as promotes the migration of the MS2 phage on the post-activated carbon cartridge that was placed in the last unit of the water purifier system, which could increase the pathogen transmission risks in drinking water supplies. The bacterial community structures of the cartridge materials and cartridge effluents from each unit were analyzed by 16S rRNA gene sequencing, which revealed distinct microbial profiles of the different purifiers. Environmental conditions such as pH, nutrient availability, materials, and operational parameters can affect the composition of bacterial communities. Scanning electron microscopy-energy-dispersive X-ray spectroscopy (SEM-EDS) was used to examine the surface morphology of the membranes after they were exposed to water contaminants, which demonstrated that the inherent differences in the membrane structure influenced the retention of pollutants and microorganisms on the surfaces. In summary, this study demonstrates that both NF and RO water purifiers can significantly reduce the presence of various enteric and opportunistic pathogenic bacteria in drinking water, leading to safer potable water, whereas UF water purifiers may have certain risks owing to their UF membranes and post-activated carbon. In addition, secondary microbial contamination may be introduced by the post-activated carbon units of water purifiers, especially after long-term usage. Therefore, we concluded that addressing the secondary microbial pollution caused by post-activated carbon after prolonged use and long-term shutdown is essential for maintaining the safety and quality of drinking water.

Silver oxide integrated ionic polymer composite for wearable sensing and water purification

Integrating metal nanoparticles (NPs) with ionic polymer blends/composites showed immense interest for their potential in wearable sensors, soft robotic arms, flexible man-machine interfaces of biomedical devices, and water purification applications. However, conventional NPs attached ionic polymer composites exhibit limitations such as low sensitivity (ΔR/R), low total dissolved solids (TDS) reduction, and low phosphate (PO4-P) removal rate. Herein, ionic polymer composites (IPCs) using flower-shaped silver oxide (Ag2O) attached Poly (vinylidene fluoride) (PVDF)/ polyvinylpyrrolidone (PVP)/ionic liquid (IL) were designed and developed for wearable sensing and water purification. The IPCs demonstrated remarkably high ΔR/R values of 50, 10, and 3.5 corresponding to the wrist movement of 50°, finger movement of 180°, and chin movements respectively. The Ag2O-based IPC recorded a significant reduction of TDS from sewage water from 3405 ppm to 1035 ppm, elevated the dissolved oxygen (DO) levels in the sewage water from 1.2 mg/l to 6.8 mg/l, and removed approximately 87.38 % phosphate from sewage water. Due to the uniform distribution of Ag2O within pores of IPC, it demonstrated enhanced performance for wearable and wastewater treatment applications.

Industrial Testing of a Hybrid Technology for Water Purification from the Oka River Using the Method of Charcoalization with Powdered Sorbent

The development of the industrial sector and the increase in production capacity have a positive effect on the economic situation of the country, but not on environmental safety. Insufficiently purified and polluted wastewater is constantly discharged into water sources, the amount of which directly depends on the industrial development of the region. Thus, the anthropogenic load on the Oka River affects the composition of water in the source, there are often bursts of instantaneous emissions, as well as the flowering of phytoplankton in the summer. The latter further significantly reduce the efficiency of water purification to drinking quality. Therefore, the development of technologies that will be able to maintain purification at the required level is an urgent task. The article presents the method of charcoalization, which allows to neutralize pollution in a short time and improve the water treatment quality. An industrial experiment of the developed technology was carried out at an operating water treatment plant with testing of two extreme do-sages of sorption material. The optimal dose of coal pulp was determined, the impact on significant purification performance was described, and the technological solutions have been developed to determine the point of coal pulp input and the dosage multiplicity. The conducted research has made it possible to expand knowledge in the field of drinking water preparation and to determine significant water parameters that are affected by the sorption purification method.

Recent Progress in Photocatalytic Applications of Electrospun Nanofibers: A Review.

Electrospun fiber-based photocatalysts demonstrate significant potential in addressing global environmental and energy challenges, primarily due to their high specific surface areas and unique properties. This review examines recent advances in the application of these materials in photocatalytic processes, with a particular focus on water splitting and hydrogen production. The principles of the electrospun method are described in detail, along with the operating parameters, material characteristics, and environmental conditions that affect the fiber formation. Additionally, the review discusses the challenges, advantages, and future prospects of photocatalysts incorporating carbon materials, metals, semiconductors, and hybrid structures with improved performance. These materials have the potential to significantly improve the efficiency of hydrogen energy production, water purification, and CO2 recovery, highlighting their importance in engineering sciences.

Honeycomb Cell Structures Formed in Drop-Casting CNT Films for Highly Efficient Solar Absorber Applications.

This study investigates the process of using multi-walled carbon nanotube (MWCNT) coatings to enhance lamp heating temperatures for solar thermal absorption applications. The primary focus is studying the effects of the self-organized honeycomb structures of CNTs formed on silicon substrates on different cell area ratios (CARs). The drop-casting process was used to develop honeycomb-structured MWCNT-coated absorbers with varying CAR values ranging from ~60% to 17%. The optical properties were investigated within the visible (400-800 nm) and near-infrared (934-1651 nm) wavelength ranges. Although fully coated MWCNT absorbers showed the lowest reflectance, honeycomb structures with a ~17% CAR achieved high-temperature absorption. These structures maintained 8.4% reflectance at 550 nm, but their infrared reflection dramatically increased to 80.5% at 1321 nm. The solar thermal performance was assessed throughout a range of irradiance intensities, from 0.04 W/cm2 to 0.39 W/cm2. The honeycomb structure with a ~17% CAR value consistently performed better than the other structures by reaching the highest absorption temperatures (ranging from 52.5 °C to 285.5 °C) across all measured intensities. A direct correlation was observed between the reflection ratio (visible: 550 nm/infrared: 1321 nm) and the temperature absorption efficiency, where lower reflection ratios were associated with higher temperature absorption. This study highlights the significant potential for the large-scale production of cost-effective solar thermal absorbers through the application of optimized honeycomb-structured absorbers coated with MWCNTs. These contributions enhance solar energy efficiency for applications in water heating and purification, thereby promoting sustainable development.

Hydrogen bonding network in the electrical double layer mediates fast proton skipping to Get Rid of Fenton reaction pH dependence enables highly efficient alkaline water purification

A fundamental scientific quandary in environmental has always been the pH dependence in Fenton reaction, that is, the reaction kinetics decreases by approximately 1–3 orders of magnitude upon transitioning from an acidic to an alkaline state. Here, we discovered that protons significantly contribute to the Fenton reaction through an examination of the reaction's interfacial behavior characteristics. Proton transfer mediated by hydrogen bond network connectivity in the electric double layer is responsible for the pH dependence of Fenton reaction kinetics. On this basis, the surface potential of Fenton reaction catalyst was modified to optimize the distribution of H2O in the electrical double layer, enhancing the connectivity of the interfacial hydrogen bond network and providing a fast channel for rapid proton transfer. The consecutive hydrogen bond network mediates rapid proton hopping, increasing the proton concentration in the Helmholtz layer, and consequently promoting the proton conductivity from 5.38×10−7 S·cm−2 to 4.35×10−6 S·cm−2 in alkaline conditions for Fenton reaction. Meanwhile, the kinetics reaction rate was improved 20 times, and the pH dependence was reduced from 70.9 % to 12.6 %. This discovery clarifies the key role of the interfacial hydrogen bond network and proton transfer in Fenton reaction kinetics pH dependence. It provides new theories and methods for achieving alkaline high Fenton reaction kinetics.

Assessment of biocidal efficacy of zinc oxide-zeolite nanocomposites as a novel water disinfectant against commercial disinfectants used in water purification

Water microbial contamination is a serious issue that poses a risk to both animal and human health. One hundred and twenty water were samples collected from main water source and drinkers from a poultry farm. Different bacterial pathogens were isolated from water sources. Escherichia (E.) coli, Pseudomonas (P.) aureoginosa, (Salmonella) Salmonella (s). Typhimurim, Aeromonas (A.) hydrophila at different percentages. Variable degree of bacterial resistance to some commercial disinfectants commonly used to disinfect water system (iodine, terminator and H2O2). Nanoparticles were used to control bacteria in water. About the safety investigation for the prepared nanomaterials, the work results demonstrated that zinc oxide (ZnO) nanoparticles (NPs) exhibit the highest safety profile among the manufactured materials. The median fatal dose (LD50) for ZnO NPs was determined to be 3709 mg/kg body weight. In comparison, the LD50 values for zeolites and nanocomposites were 3251 mg/kg and 2658 mg/kg, respectively. Therapeutic dosages were estimated based on the LD50. Zeolite NPs, ZnO NPs and ZnO/zeolite NPs showing promising results in control of those bacteria. It was concluded that the escalating resistance of bacteria to disinfectants have led to a need to find alternative such as nanoparticles that proved promising results in control of pathogens, particularly it showed a safe effect on laboratory animals.

Antibacterial bio pores as a river flow filter for the development of "Ndeso Park" water tourism

The realization of the full potential of natural resources in each village for the benefit of the local community has been observed as a significant challenge. The national village-owned enterprises program encourages villages to optimize the utilization of their existing natural and human resources with the objective of fostering their economic independence. The program entails the optimization of the national village-owned enterprises program in the tourism sector, specifically in the context of Taman Ndeso. The objective of this community service activity is to provide technological assistance and address the issue of river water filtration as a pool water source. The impetus for this activity is the declining tourism activities at Taman Ndeso due to the presence of turbid water in the pool, which was deemed unsuitable for use. The activity is realized through the construction of a water purification filtration system to produce clean and healthy water. The antibacterial biopores are applied as filtration technology. This technology is designed to capture bacteria from river water that flow into the pond. This research adopted the direct exploration method, which was divided into a number of stages, including planning and preparation, implementation, evaluation, and reporting. The research outcome manifests into the restoration of the Taman Ndeso water tourism pool, which will be capable of attracting tourists and reviving village income to the maximum extent possible, with the management of the village-owned business entity.

Effective removal of Pb(II) ions using Fe3O4/MgO adsorbent: A comprehensive study  

The effective removal of heavy metal ions, particularly Pb(II), from contaminated water sources remains a pressing environmental concern. This study explores the potential of Fe3O4/MgO nanocomposites as an efficient adsorbent for selective Pb(II) removal. The Fe3O4/MgO nanocomposite was synthesized using a controlled sol-gel method and characterized using various techniques. X-ray diffraction (XRD) analysis confirmed the presence of cubic MgO and cubic Fe3O4. Pb(II) adsorption induced a crystallographic transformation, forming hexagonal Mg(OH)2 crystals, indicating interaction with the adsorbent. Scanning Electron Microscope (SEM) analysis revealed pyramid-like and irregular crystal morphologies. Pyramid-like structures provided a larger surface area and active sites for effective Pb(II) interaction, while irregular crystal particles, representing magnetic Fe3O4, contributed to stability and dispersibility. Vibrating sample magnetometer (VSM) results confirmed superparamagnetic behaviour with a saturation magnetization of 32.02 emu g-1, indicating potential for magnetic separation and recovery in various wastewater treatment applications. Adsorption experiments utilized optimized conditions: an initial concentration of 600 mg L-1, adsorbent dosage of 0.25 g L-1, pH of 7, and 120 minutes of reaction time. The Fe3O4/MgO nanocomposite exhibited exceptional performance with a remarkable 99.98% removal efficiency and a high adsorption capacity of 2399.44 mg g-1. These impressive results underscore the outstanding adsorption potential of the nanocomposite. Adsorption kinetics followed the pseudo-second-order model (R2 = 0.99), confirming suitability for Pb(II) removal. The Freundlich model indicated a heterogeneous surface with different adsorption sites. Overall, the Fe3O4/MgO nanocomposite exhibits potential as a cost-effective, environmentally friendly adsorbent for removing Pb(II) ions, providing a promising solution for water purification and environmental remediation.

Clays-based geopolymers: a sustainable application as adsorbent of cytostatic drugs for water purification

The administration of cytostatic drugs in chemotherapy is steadily increasing, triggering thus a risk to the environment. Identifying powerful ways to effectively remove these hazardous pollutants from hospital and effluent wastewater before they discharge into the aquatic environment remains a critical and challenging task. Adsorption is among the most effective ways to treat contaminated water due to the wide availability and selectivity of the adsorbents besides the simplicity and the low start-up costs of the technique. In this work, a geopolymer, elaborated from an illito-kaolinitic clay (Douiret region of Tunisia) and industrial waste (silica fume and phosphogypsum), has been tested as promising decontamination of the cytostatic drugs paclitaxel (PCX) and irinotecan (IRI) from water samples. The foamed geopolymer was characterized using X-ray diffraction, Fourier transform infrared, scanning electron microscopy and thermogravimetric analysis before and after adsorption. Adsorption batch assays were performed using different concentrations of PCX and IRI, contact times and environmental conditions. The geopolymer had an excellent removal efficiency (almost 100% for PCX and 89% for IRI) using 20 mg of adsorbent and 2.5 mg/L of each drug concentration. The characterization results showed that cytostatic drugs were adsorbed to the geopolymer through physical interactions, pore filling, electrostatic attraction and hydrogen bonding. The specific surface area and pore volume of the geopolymer were 82.23 m2/g and 0.19 cm3/g, respectively. In addition to its cost-effective properties, the geopolymer demonstrated excellent efficiency in contaminated natural samples (including influent, effluent wastewater and surface water) denoting a great application for water purification.

Microenvironment Engineering of Heterogeneous Catalysts for Liquid-Phase Environmental Catalysis.

Environmental catalysis has emerged as a scientific frontier in mitigating water pollution and advancing circular chemistry and reaction microenvironment significantly influences the catalytic performance and efficiency. This review delves into microenvironment engineering within liquid-phase environmental catalysis, categorizing microenvironments into four scales: atom/molecule-level modulation, nano/microscale-confined structures, interface and surface regulation, and external field effects. Each category is analyzed for its unique characteristics and merits, emphasizing its potential to significantly enhance catalytic efficiency and selectivity. Following this overview, we introduced recent advancements in advanced material and system design to promote liquid-phase environmental catalysis (e.g., water purification, transformation to value-added products, and green synthesis), leveraging state-of-the-art microenvironment engineering technologies. These discussions showcase microenvironment engineering was applied in different reactions to fine-tune catalytic regimes and improve the efficiency from both thermodynamics and kinetics perspectives. Lastly, we discussed the challenges and future directions in microenvironment engineering. This review underscores the potential of microenvironment engineering in intelligent materials and system design to drive the development of more effective and sustainable catalytic solutions to environmental decontamination.

Copper nanoparticles biosynthesis by Priestia megaterium and its application as antibacterial and antitumor agents

The growth of material science and technology places high importance on creating better processes for synthesizing copper nanoparticles. Thus, an easy, ecological, and benign process for producing copper nanoparticles (CuNPs) has been developed using Priestia sp. bacteria utilizing a variety of low-cost agro-industrial wastes and byproducts. The biosynthesis of CuNPs was conducted using glucose medium and copper ions salt solution, then it was replaced by utilizing low-cost agro-industrial wastes. UV–visible spectroscopy, dynamic light scattering (DLS), X-ray diffraction (XRD), High-resolution transmission electron microscope (HR-TEM), Attenuated Total Reflectance and Fourier transform infrared (ATR-FTIR), and zeta potential were used to characterize the biosynthesized CuNPs. The cytotoxicity of CuNPs using Vero -CCL-81 cell lines, and antibacterial and antitumor properties using human colon epithelial colorectal adenocarcinoma Caco-2-HTB-37 cell lines were assessed. The UV–visible and DLS studies revealed CuNPs formation, with a maximum concentration of 6.19 ppm after 48 h, as indicated by a 0.58 Surface plasmon resonance (SPR) within 450 nm and 57.73 nm particle size. The 16S rRNA gene analysis revealed that Priestia sp. isolate is closely related to Priestia megaterium and has been deposited in the NCBI GenBank with accession number AMD 2024. The biosynthesis with various agro-industrial wastes indicated blackstrap sugar cane molasses being the most effective for reducing CuNPs size to 3.12 nm owing to various reducing and stabilizing active compounds. The CuNPs were free of contaminants, with a sphere-shaped structure and a cytotoxicity assessment with an IC50 of 367.27 μg/mL. The antibacterial activity exhibited by the most susceptible bacteria were Bacillus cereus ATCC 11788 and Staphylococcus aureus ATCC 6538 with inhibition zones of 26.0 mm and 28.0 mm, respectively. The antitumor effect showed an IC50 dose of 175.36 μg/mL. Based on the findings, the current work sought to lower product costs and provide a practical solution to the environmental contamination issues brought on by the buildup of agricultural wastes. In addition, the obtained CuNPs could be applied in many fields such as pharmaceuticals, water purification, and agricultural applications as future aspects.

A low-carbon dual-functional evaporator with photothermal and catalytic properties for enhanced VOCs removal during water evaporation

Solar interface distillation technologies are widely used for seawater desalination, wastewater treatment, and clean water production. However, during evaporation, volatile organic compounds (VOCs) in the water often evaporate coincidently with the water vapor, presenting a major pollutant challenge. Combining solar evaporation with advanced oxidation processes (AOP) is a potential solution for simultaneous water purification and VOC degradation. Herein, a dual-functional sponge photothermal evaporator (MBC-SA/MS) was designed to assess the efficacy of this approach. A simple porous sponge embedded with a composite catalyst, comprising MoO3−x, BiOCl, and CNT, was able to demonstrate simultaneous photothermal evaporation and catalytic degradation. MBC-SA/MS exhibited exceptional photothermal conversion efficiency and robust catalytic activity, achieving an evaporation rate of 2.1 kg m−2 h−1 under 1.0 sun intensity. Effective mitigating of phenol emissions was observed through persulfate activation resulting in 90 % phenol degradation. Life cycle assessment (LCA) confirmed this evaporator system had low environmental impact and was sustainable. This research presents a new compelling strategy for tackling VOC pollution and simultaneously enhancing water purification via solar interfacial evaporation.

Using zero nano-valent iron/thin film composite (ZNVI/TFC) membrane for brackish water desalination and purification

This study looked at the use of synthetic Zero Nano-valent Iron (ZNVI) particles in a unique interfacial polymerization technique on a polyamide thin film PA(TF) composite membrane for the treatment and desalination of brackish wastewater. Zero nano-valent iron (ZNVI) particles were created utilizing chemical reduction technique. ZNVI/PA(TF) NCs membrane is the outcome of advancing the PA(TF) membrane by combining with different concentration of ZNVI particles into the organic phase 1,3,5-benzenetricarbonyl trichloride (TMC). ZNVI/PA(TF) NCs membranes and ZNVI particles' surface properties were examined by the use of mechanical activity, contact angle, BET, FTIR, SEM, XRD, zeta potential, TEM analysis, and EDX studies. Using a variety of salt solutions, such as NaCl, Na2SO4, MgSO4, NaHCO3, CaSO4, CaCl2, and MgCl2, the ZNVI/PA(TF) NCs membrane performance towards salt rejection, flux (at varying pressure), anti-fouling activity, and ZNVI particles stability was assessed. This work investigated the removal efficiency of four dyes: methylene blue (MB), methyl orange (MO), Congo red (CR), and malachite green oxalate (MG). The water flux of the pristine PA(TF) membrane improved from 22 to 35 L/m2.h at 15 bar, indicating a 63% flux enhancement and the NaCl rejection was improved from 88.5 to 98.6%, indicating an 11.4% rejection improvement by incorporation of 0.3 wt.% of ZNVI particles into PA(TF) matrix. The ZNVI/PA(TF) NCs membrane's separation performances were evaluated using 5000 mg/L feed solutions of various salts at 15 bar. It was discovered that the water flux and salt rejection are, respectively, 33.4, 33, 32.7, 32, 31, 30 and 29 L/m2.h for CaSO4, MgSO4, Na2SO4, NaCl, CaCl2, MgCl2, and NaHCO3, and 97.4, 97, 96.5, 96, 94, 93.2, and 92.8%. It demonstrates that the flux recovery ratio (FRR) of the ZNVI/PA(TF) NCs membrane is greater than that of pristine PA(TF) (78%), coming in at 87%. High stability and fixing of the ZNVI particles on the modified membrane surface is indicated by the low overall ZNVI particles release rate over the course of the 10-day experiment.

Unraveling the Fundamentals of Axial Coordination FeN4+1 Sites Regulating the Peroxymonosulfate Activation for Fenton-Like Activity.

Precise modulation of the axial coordination microenvironment in single-atom catalysts (SACs) to enhance peroxymonosulfate (PMS) activation represents a promising yet underexplored approach. This study introduces a pyrolysis-free strategy to fabricate SACs with well-defined axial-FeN4+1 coordination structures. By incorporating additional out-of-plane axial nitrogen into well-defined FeN4 active sites within a planar, fully conjugated polyphthalocyanine framework, FeN4+1 configurations are developed that significantly enhance PMS activation. The axial-FeN4+1 catalyst excelled in activating PMS, with a high bisphenol A (BPA) degradation rate of 2.256 min-1, surpassing planar-FeN4/PMS systems by 6.8 times. Theoretical calculations revealed that the axial coordination between N and the Fe sites forms an optimized axial FeN4+1 structure, disrupting the electron distribution symmetry of Fe and optimizing the electron distribution of the Fe 3d orbital (increasing the d-band center from -1.231 to -0.432eV). Consequently, this led to an enhanced perpendicular adsorption energy of PMS from -1.79 to -1.82eV and reduced energy barriers for the formation of the key reaction intermediate (O*) that generates 1O2. This study provides new insights into PMS activation through the axial coordinated engineering of well-defined SACs in water purification processes.

Chalky limestone as sustainable water purification from eriochrome black T: kinetics, isotherm, and equilibrium

Chalky limestone as sustainable water purification from eriochrome black T: kinetics, isotherm, and equilibrium

Bioinspired Hydrophobicity via Temperature-Induced Phase Separation of Beeswax: A Pathway for Developing Cellulose Nanofiber-Based Adsorbents for the Removal of Conventional Tetracycline Tablets.

Cellulose nanofiber-based aerogels (CNFAs) hold immense promise across diverse fields, but their innate hydrophilicity and structural fragility in water have constrained their utility in water purification. This study introduces a green approach to induce hydrophobicity into CNFAs via thermally induced phase separation (TIPS) of beeswax, which was adhered to the nanofiber by hydrogen bonding and hydrophobic-hydrophobic interactions. The fabricated aerogel was characterized by using FTIR, SEM, XRD, TGA, contact angle, BET, and compression test. The resulting beeswax cellulose nanofiber-based aerogels (BCNFAs) possess a highly porous structure and extremely low density, enabling the aerogels to self-float and facilitate practical applications and recycling. Due to these remarkable characteristics, BCNFAs had excellent adsorption capacity within 10 min to effectively remove tetracycline (TC) from water with an adsorption capacity of 31.6 mg/g. The demonstrated methodology to induce hydrophobicity in CNFAs via TIPS of beeswax on CNFAs could be an eco-friendly and scalable approach for the fabrication of robust BCNFAs without using any toxic chemicals. So far, this is the first report on to make robust hydrophobic CNFAs by employing TIPS of beeswax while maintaining the porosity of CNFAs, which is highly desirable for effective TC tablet adsorption from water in the present context. The demonstrated work has commercial potential as it focuses on the practical utility of the modified aerogel for adsorbing conventional tetracycline tablets, rather than exclusively targeting the pharmaceutical ingredient alone.