Potential of Capparis decidua plant and eggshell composite adsorbent for effective removal of anionic dyes from aqueous medium.

The presence of hazardous dyes in wastewater poses significant threats to both ecosystems and the natural environment. Conventional methods for treating dye-contaminated water have several limitations, including high costs and complex operational processes. This study investigated a sustainable bio-sorbent composite derived from the Capparis decidua plant and eggshells, and evaluated its effectiveness in removing anionic dyes namely tartrazine (E-102), methyl orange (MO), and their mixed system. The research examines the influence of initial concentration, contact time, pH, adsorbent dosage, and temperature on the adsorption properties of anionic dyes. Optimal removal of tartrazine (E-102), methyl orange (MO), and their mixed system was achieved at a pH of 3. The equilibrium was achieved at 80 min for MO and mixed systems, and 100 min for E-102. The adsorption process showed an exothermic nature, indicating reduced capacity with increasing temperature, consistent with heat release during adsorption. Positive entropy values indicated increased disorder at the solid-liquid interface, attributed to molecular rearrangements and interactions between dye molecules and the adsorbent. Isotherm analysis using Langmuir, Freundlich, Temkin, and Redlich-Peterson models revealed that the Langmuir model best fit the experimental data. The maximum adsorption capacities of 50.97 mg/g, 52.24 mg/g, and 56.23 mg/g were achieved for E-102, MO, and the mixed system under optimized conditions, respectively. The pseudo-second-order kinetic model demonstrated the best fit, indicating that adsorption occurs through physical and chemical interactions such as electrostatic attraction, pore filling, and hydrogen bonding. Hence, the developed bio-sorbent could be a sustainable and cost-effective solution for the treatment of anionic dyes from industrial effluents.

Comprehensive review on pH and temperature-responsive polymeric adsorbents: Mechanisms, equilibrium, kinetics, and thermodynamics of adsorption processes for heavy metals and organic dyes.

Wastewater treatment technologies have been developed to address the health and environmental risks associated with toxic and cancer-causing dyes and heavy metals found in industrial waste. The most commonly used method to mitigate and treat such effluents is adsorption, which is favored for its high efficiency, low costs, and ease of operation. However, traditional adsorbents have limitations in terms of regeneration and selectivity compared to smart adsorbents. Smart polymeric adsorbents, on the other hand, can undergo physical and chemical changes in response to external factors like temperature and pH, enabling a selective adsorption process. These adsorbents can be easily regenerated and reused with minimal generation of secondary pollutants during desorption. The unique properties acquired by stimuli-responsive adsorbents have encouraged researchers to investigate their potential for the selective and efficient removal of organic dyes and heavy metals. This comprehensive review focuses on two common stimuli, pH and temperature, discussing the fabrication methods and characteristics of smart adsorbents responsive to these factors. It also provides an overview of the mechanisms, isotherms, kinetics, and thermodynamics of the adsorption process for each type of stimuli-responsive adsorbent. Finally, the review concludes with discussions on future perspectives and considerations.

Photoelectrochemical advanced oxidation processes for simultaneous removal of antibiotics and heavy metal ions in wastewater using 2D-on-2D WS2@CoFe2O4 heteronanostructures.

The presence of antibiotics in water poses significant threats to both human health and the environment. Addressing this issue requires the effective treatment of medical wastewater. Photoelectrochemical advanced oxidation processes (PEAOPs) are emerging as promising solutions for wastewater treatment. This process utilizes photocatalysts to convert charge carriers into reactive species such as hydroxyl radicals and superoxide ions, which are essential for degrading pollutants in wastewater. However, limitations in charge carrier separation and transport have hindered the efficiency of photoelectrochemical advanced oxidation processes. To overcome these limitations, we designed WS2@CoFe2O4 heterojunctions, optimizing their energy levels to enhance charge transport and separation. This improvement significantly increased the oxidation of antibiotics such as amoxicillin and azithromycin. Multiple reactions occurred at the WS2@CoFe2O4 heterojunctions during photoelectrochemical advanced oxidation processes, leading to the impressive degradation of up to 99% of antibiotics under visible light irradiation at 0.8 V. Urea and H2O2 acted as oxidation agents within photoelectrochemical advanced oxidation processes, amplifying the generation of hydroxyl radicals and superoxide ions, further enhancing antibiotic oxidation. Moreover, the WS2@CoFe2O4 photoanode efficiently oxidized toxic antibiotics while converting As(III) into the less harmful As(V). Crucially, recyclability tests confirmed the robustness of the WS2@CoFe2O4 photoanode, ensuring its suitability for prolonged use in photoelectrochemical advanced oxidation processes. Integrating WS2@CoFe2O4 photoanodes into water purification systems can enhance efficiency, reduce energy consumption, and improve economic viability. This technology's scalability and its ability to protect ecosystems while conserving water resources make it a promising solution for addressing the critical issue of antibiotic pollution in water environments.

Facile Preparation of Magnetic CuFe2O4 on Sepiolite/GO Nanocomposites for Efficient Removal of Pb(II) and Cd(II) from Aqueous Solution.

CuFe2O4 nanoparticles were synthesized and immobilized on sepiolite fibers and graphene oxide sheets, producing a CuFe2O4/sepiolite/GO (CFSG) nanocomposite via a facile single-pot method. The synthesized nanocomposite was characterized using TEM, FTIR, SEM-EDX, XRD, and TGA techniques to determine its composition, structure, and thermal stability. The adsorptive removal of Pb(II) and Cd(II) heavy metal ions from aqueous solutions was studied using the synthesized CFSG nanocomposite. Adsorption parameters such as CFSG loading, pH, contact time, and temperature were investigated. The CFGS nanocomposite showed a higher Pb(II) removal (qm = 238.1 mg/g) compared to Cd(II) (qm = 14.97 mg/g) in a Pb(II) and Cd(II) binary system. The Pb(II) and Cd(II) adsorption fitted well with the Langmuir model, followed by the pseudo-second-order model, and was found spontaneous. Adsorption thermodynamic analysis showed that the Pb(II) adsorption process was exothermic while Cd(II) adsorption was endothermic. The CuFe2O4 nanoparticles on the CFSG surface could facilitate the adsorption of heavy metal ions through electrostatic interaction and complexation processes.

Advancing water treatment sustainability: Investigating electrified Ti3C2Tx composite membranes for minimizing microplastic fouling.

The overuse of plastics has led to a large influx of microplastics (MPs) in water bodies and water/wastewater treatment plants. Coupled with the ongoing water crisis, this poses a threat to freshwater availability as MPs disrupt the operation of these plants. MPs cause severe fouling of low-pressure membrane technologies such as ultrafiltration (UF) due to the strong adhesion between MPs and the membrane surface. An electrified membrane-based technology is suggested as an alternative MP fouling mitigation strategy. In this study, composite membranes of sulfonated polyethersulfone (SPES)/MXene (Ti3C2Tx) were fabricated and evaluated as a promising candidate for mitigating fouling of MPs. The described SPES/Ti3C2Tx composite membrane was designed to improve important physiochemical properties such as conductivity without affecting water flux. The membranes were tested under different electrical potentials to find an optimal strategy to reduce MP fouling. The performance tests showed that the flux increased from 42 L m-2. h-1 at 0 V to 49 L m-2. h-1 at 2 V due to electrostatic repulsion when 5 wt% Ti3C2Tx was used as a result of the applied electric potential. In addition, it was shown that intermittent applied voltage using "30 min ON: 60 min OFF" mode resulted in more stable water flux due to in-situ coagulant formation and cleaning. This study illustrates the potential of MXene-based membranes for mitigating MP fouling and paves the way for future research on membrane materials that can enhance system performance.

An advanced photo-oxidation process for pharmaceuticals using plasmon-assisted Ag-CoFe2O4 photocatalysts.

The discharge of amoxicillin (AMX) from pharmaceutical intermediates has adverse effects on aquatic ecosystems. The elimination of AMX requires advanced oxidation processes (AOPs) that utilize high-performance photocatalysts. Furthermore, the design of highly visible light photocatalysts for AOPs demands both cost-effectiveness and efficiency. In this work, a plasmon-assisted visible light photocatalyst of 2D Ag-CoFe2O4 nanohybrids was successfully synthesized and characterized with several analytical tools to degrade AMX in aqueous solutions through advanced AOPs. The results showed that the Ag-CoFe2O4 nanohybrids had excellent photocatalytic activity and stability, which could efficiently reduce the AMX concentration by 99% within 70 min under visible light irradiation. In particular, CoFe2O4 and Ag have an interfacial contact that prevents electron-hole pair recombination more effectively than pure CoFe2O4, which results in electrons in its conduction band (CB) migrating to metallic Ag sites. Thus, charge transfers between the two materials are more efficient, leading to higher photocatalytic oxidation of AMX. Furthermore, the surface plasmon of Ag nanoparticles are excited by their plasmonic resonance, which increases the absorption of visible light. The plasmon-assisted visible light photocatalyst could replace expensive and energy-intensive advanced oxidation processes (AOPs). AOPs pathways associated with AMX have been discussed in detail. The HPLC chromatogram clearly showed AMX was oxidized by four-membered B-lactam ring opening and hydroxylation with •OH. 2D Ag-CoFe2O4 heterostructure was found to be efficient, selective, and cost-effective for the degradation of several pharmaceutical compounds. Additionally, it was found to be eco-friendly and sustainable, making it a viable alternative to AOPs.

Phosphorus-modified copper ferrite (P-CuFe2O4) nanoparticles for photocatalytic ozonation of lomefloxacin.

Phosphorus-modified copper ferrite (P-CuFe2O4) nanoparticles were prepared by a simple sol-gel auto-combustion process and used for the photocatalytic ozonation of lomefloxacin (LOM). The morphology, crystallinity, and structure of the synthesized CuFe2O4 and P-CuFe2O4 nanoparticles were investigated using various techniques. The high-performance liquid chromatography (HPLC) analysis revealed that the degradation of LOM achieved a 99% reduction after a duration of 90 min in the photocatalytic ozonation system. In accordance with the charge-to-mass ratio, four intermediates were proposed with the help of their fragments obtained in LC-MS/MS. The degradation kinetics of lomefloxacin followed a pseudo-first order reaction, and the degradation mechanism was proposed based on the results. P0.035Cu0.965Fe2O4 showed the highest total organic carbon (TOC) removal with 20.15% in 90 min, highest specific surface area and the highest fluoride and ammonium production using the ion chromatography (IC). The experimental results obtained from the electron paramagnetic resonance (EPR) analysis indicated that the modified P-CuFe2O4 samples exhibited significantly elevated levels of superoxide (.O2-) production compared to the CuFe2O4 samples. The findings of this study demonstrate that the introduction of phosphorus modification into the copper ferrite photocatalyst led to an augmentation of both the specific surface area and the total pore volume. Furthermore, the incorporation of phosphorus served to promote the efficient separation of electron-hole pairs by effectively trapping electrons in the conduction band, hence enhancing the degradation efficiency.

Simultaneous adsorption of methylene blue and amoxicillin by starch-impregnated MgAl layered double hydroxide: Parametric optimization, isothermal studies and thermo-kinetic analysis.

Textile and pharmaceutical effluents contain significant amounts of dyes and antibiotics, which pose a serious threat to the ecosystem when discharged directly. Therefore, they should be treated by facile treatment techniques using low-cost materials. Layered double hydroxide (LDH) and its hybrids have emerged as robust and economic adsorbents for water treatment. Herein, magnesium/aluminum LDH and its starch-based composite were synthesized by a co-precipitation technique. The physicochemical features of the developed adsorbents were thoroughly characterized using various analytical tools. The developed materials were tested for the eradication of methylene blue (MB) and amoxicillin (AMX) in batch mode adsorption by varying operating conditions. Adsorption performance depends on the solution's pH. Under optimum adsorption conditions of pH 11, adsorbent dosage of 50 mg/L, and treatment time of 120 min, starch-impregnated MgAl-LDH exhibited maximum MB and AMX adsorption capacities of 114.94 and 48.08 mg/g, respectively. The adsorption mechanism states that hydrogen bonds and weak van der Waals forces are responsible for the removal of pollutants by the developed materials. Moreover, equilibrium and kinetic studies revealed that the removal of dye and antibiotic followed the Freundlich and Langmuir models with the pseudo-second-order reaction kinetics, respectively. The spent adsorbents were regenerated using 0.1 M HCl (for MB) and methanol (for AMX) eluent, and reusability studies ensured that the developed adsorbents retained their performance for up to four consecutive adsorption/desorption cycles. MgAl-LDH and its starch-based hybrid could thus be used to effectively remove organic contaminants from wastewater streams on a commercial scale.

Molecular Guide for Selecting Green Deep Eutectic Solvents with High Monosaccharide Solubility for Food Applications.

Monosaccharides play a vital role in the human diet due to their interesting biological activity and functional properties. Conventionally, sugars are extracted using volatile organic solvents (VOCs). Deep eutectic solvents (DESs) have recently emerged as a new green alternative to VOCs. Nonetheless, the selection criterion of an appropriate DES for a specific application is a very difficult task due to the designer nature of these solvents and the theoretically infinite number of combinations of their constituents and compositions. This paper presents a framework for screening a large number of DES constituents for monosaccharide extraction application using COSMO-RS. The framework employs the activity coefficients at infinite dilution (γi∞) as a measure of glucose and fructose solubility. Moreover, the toxicity analysis of the constituents is considered to ensure that selected constituents are safe to work with. Finally, the obtained viscosity predictions were used to select DESs that are not transport-limited. To provide more insights into which functional groups are responsible for more effective monosaccharide extraction, a structure-solubility analysis was carried out. Based on an analysis of 212 DES constituents, the top-performing hydrogen bond acceptors were found to be carnitine, betaine, and choline chloride, while the top-performing hydrogen bond donors were oxalic acid, ethanolamine, and citric acid. A research initiative was presented in this paper to develop robust computational frameworks for selecting optimal DESs for a given application to develop an effective DES design strategy that can aid in the development of novel processes using DESs.

Natural deep eutectic solvents for Ultrasonic-Assisted extraction of nutritious date Sugar: Molecular Screening, Experimental, and prediction.

The aim of this study is to develop an environmentally friendly and effective method for the extraction of nutritious date sugar using natural deep eutectic solvents (NADES) and ultrasound-assisted extraction (USAE). The careful design of a suitable NADES-USAE system was systematically supported by COSMO-RS screening, response surface method (RSM) and artificial neural network (ANN). Initially, 26 natural hydrogen bond donors (HBDs) were carefully screened for sugar affinity using COSMO-RS. The best performing HBDs were then used for the synthesis of 5 NADES using choline chloride (ChCl) as HBA. Among the synthesized NADES, the mixture of ChCl, citric acid (CA) and water (1:1:1 with 20 wt% water) resulted in the highest sugar yield of 78.30 ± 3.91 g/100 g, which is superior to conventional solvents such as water (29.92 ± 1.50 g/100 g). Further enhancements using RSM and ANN led to an even higher sugar recovery of 87.81 ± 2.61 g/100 g, at conditions of 30 °C, 45 min, and a solvent to DFP ratio of 40 mL/g. The method NADES-USAE was then compared with conventional hot water extraction (CHWE) (61.36 ± 3.06) and showed 43.1% higher sugar yield. The developed process not only improves the recovery of the nutritious date sugar but also preserves the heat-sensitive bioactive compounds in dates, making it an attractive alternative to CHWE for industrial utilization. Overall, this study shows a promising approach for the extraction of nutritive sugars from dates using environmentally friendly solvents and advanced technology. It also highlights the potential of this approach for valorizing underutilized fruits and preserving their bioactive compounds.

Phase inverted hydrophobic polyethersulfone/iron oxide-oleylamine ultrafiltration membranes for efficient water-in-oil emulsion separation.

Exploration and transportation of oil offshore can result in oil spills that cause a wide range of adverse environmental consequences and destroy aquatic life. Membrane technology outperformed the conventional procedures for oil emulsion separation due to its improved performance, reduced cost, removal capacity, and greater eco-friendly. In this study, a hydrophobic iron oxide-oleylamine (Fe-Ol) nanohybrid was synthesized and incorporated into polyethersulfone (PES) to prepare novel PES/Fe-Ol hydrophobic ultrafiltration (UF) mixed matrix membranes (MMMs). Several characterization techniques were performed to characterize the synthesized nanohybrid and fabricated membranes, including scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), Fourier transform-infrared spectroscopy (FT-IR), X-ray diffraction (XRD), thermal gravimetric analysis (TGA), contact angle, and zeta potential. The membranes' performance was assessed using a surfactant-stabilized (SS) water-in-hexane emulsion as a feed and a dead-end vacuum filtration setup. The incorporation of the nanohybrid enhanced the hydrophobicity, porosity, and thermal stability of the composite membranes. At 1.5 wt% Fe-Ol nanohybrid, the modified PES/Fe-Ol MMM membranes reported high water rejection efficiency of 97.4% and 1020.4 LMH filtrate flux. The re-usability and antifouling properties of the membrane were examined over five filtration cycles, demonstrating its great potential for use in water-in-oil separation.

SARS-CoV-2 detection and inactivation in water and wastewater: review on analytical methods, limitations and future research recommendations.

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been detected in wastewater. Wastewater-based epidemiology (WBE) is a practical and cost-effective tool for the assessment and controlling of pandemics and probably for examining SARS-CoV-2 presence. Implementation of WBE during the outbreaks is not without limitations. Temperature, suspended solids, pH, and disinfectants affect the stability of viruses in wastewater. Due to these limitations, instruments and techniques have been utilized to detect SARS-CoV-2. SARS-CoV-2 has been detected in sewage using various concentration methods and computer-aided analyzes. RT-qPCR, ddRT-PCR, multiplex PCR, RT-LAMP, and electrochemical immunosensors have been employed to detect low levels of viral contamination. Inactivation of SARS-CoV-2 is a crucial preventive measure against coronavirus disease 2019 (COVID-19). To better assess the role of wastewater as a transmission route, detection, and quantification methods need to be refined. In this paper, the latest improvements in quantification, detection, and inactivation of SARS-CoV-2 in wastewater are explained. Finally, limitations and future research recommendations are thoroughly described.

Prospects of microalgae in nutraceuticals production with nanotechnology applications.

Nutraceutical supplements provide health benefits, such as fulfilling the lack of nutrients in the human body or being utilized to treat or cure certain diseases. As the world population is growing, certain countries are experiencing food crisis challenges, causing natural foods are not sustainable to be used for nutraceutical production because it will require large-scale of food supply to produce enriched nutraceutics. The high demand for abundant nutritional compounds has made microalgae a reliable source as they can synthesize high-value molecules through photosynthetic activities. However, some microalgae species are limited in growth and unable to accumulate a significant amount of biomass due to several factors related to environmental conditions. Therefore, adding nanoparticles (NPs) as a photocatalyst is considered to enhance the yield rate of microalgae in an energy-saving and economical way. This review focuses on the composition of microalgal biomass for nutraceutical production, the health perspectives of nutritional compounds on humans, and the application of nanotechnology on microalgae for improved production and harvesting. The results obtained show that microalgal-based compounds indeed have better nutrients content than natural foods. However, nanotechnology must be further comprehended to make them non-hazardous and sustainable.

Spray dried date fruit extract with a maltodextrin/gum arabic binary blend carrier agent system: Process optimization and product quality.

Bioactive compounds can be protected from degradation through encapsulation, increasing their bioavailability and shelf life. Spray drying is an advanced encapsulation technique mainly used for the processing of food-based bioactives. In this study, Box-Behnken design (BBD)-based response surface methodology (RSM) was used to study the effects of combined polysaccharide carrier agents and other spray drying parameters on encapsulating date fruit sugars obtained from a supercritical assisted aqueous extraction. The spray drying parameters were set at various levels: Air inlet temperature (150-170 °C), feed flow rate (3-5 mL/min), and carrier agent concentration (30-50 %). Under the optimized conditions (inlet temperature of 170 °C, the feed flow rate of 3 mL/min, and carrier agent concentration of 44 %), a maximum sugar powder yield of 38.62 % with 3.5 % moisture, 18.2 % hygroscopicity and 91.3 % solubility was obtained. The tapped density and particle density of the dried date sugar were estimated as 0.575 g cm-3 and 1.81 g cm-3, respectively, showing its potential for easy storage. In addition, scanning electron microscope (SEM) and X-ray diffraction (XRD) analysis revealed better microstructural stability of the fruit sugar product, which is essential for commercial applications. Thus, the hybrid carrier agent system (maltodextrin and gum arabic) can be considered a potential carrier agent for producing stable date sugar powder with longer shelf-life and desirable characteristics in the food industry.

Critical Properties of Ternary Deep Eutectic Solvents Using Group Contribution with Extended Lee-Kesler Mixing Rules.

One of the most commonly used molecular inputs for ionic liquids and deep eutectic solvents (DESs) in the literature are the critical properties and acentric factors, which can be easily determined using the modified Lydersen-Joback-Reid (LJR) method with Lee-Kesler mixing rules. However, the method used in the literature is generally applicable only to binary mixtures of DESs. Nevertheless, ternary DESs are considered to be more interesting and may provide further tailorability for developing task-specific DESs for particular applications. Therefore, in this work, a new framework for estimating the critical properties and the acentric factor of ternary DESs based on their molecular structures is presented by adjusting the framework reported in the literature with an extended version of the Lee-Kesler mixing rules. The presented framework was applied to a data set consisting of 87 ternary DESs with 334 distinct compositions. For validation, the estimated critical properties and acentric factors were used to predict the densities of the ternary DESs. The results showed excellent agreement between the experimental and calculated data, with an average absolute relative deviation (AARD) of 5.203% for ternary DESs and 5.712% for 260 binary DESs (573 compositions). The developed methodology was incorporated into a user-friendly Excel worksheet for computing the critical properties and acentric factors of any ternary or binary DES, which is provided in the Supporting Information. This work promotes the creation of robust, accessible, and user-friendly models capable of predicting the properties of new ternary DESs based on critical properties, thus saving time and resources.

A Review of Advanced Multifunctional Magnetic Nanostructures for Cancer Diagnosis and Therapy Integrated into an Artificial Intelligence Approach.

The new era of nanomedicine offers significant opportunities for cancer diagnostics and treatment. Magnetic nanoplatforms could be highly effective tools for cancer diagnosis and treatment in the future. Due to their tunable morphologies and superior properties, multifunctional magnetic nanomaterials and their hybrid nanostructures can be designed as specific carriers of drugs, imaging agents, and magnetic theranostics. Multifunctional magnetic nanostructures are promising theranostic agents due to their ability to diagnose and combine therapies. This review provides a comprehensive overview of the development of advanced multifunctional magnetic nanostructures combining magnetic and optical properties, providing photoresponsive magnetic platforms for promising medical applications. Moreover, this review discusses various innovative developments using multifunctional magnetic nanostructures, including drug delivery, cancer treatment, tumor-specific ligands that deliver chemotherapeutics or hormonal agents, magnetic resonance imaging, and tissue engineering. Additionally, artificial intelligence (AI) can be used to optimize material properties in cancer diagnosis and treatment, based on predicted interactions with drugs, cell membranes, vasculature, biological fluid, and the immune system to enhance the effectiveness of therapeutic agents. Furthermore, this review provides an overview of AI approaches used to assess the practical utility of multifunctional magnetic nanostructures for cancer diagnosis and treatment. Finally, the review presents the current knowledge and perspectives on hybrid magnetic systems as cancer treatment tools with AI models.

Ag-CuO-Decorated Ceramic Membranes for Effective Treatment of Oily Wastewater.

Although ultrafiltration is a reliable method for separating oily wastewater, the process is limited by problems of low flux and membrane fouling. In this study, for the first time, commercial TiO2/ZrO2 ceramic membranes modified with silver-functionalized copper oxide (Ag-CuO) nanoparticles are reported for the improved separation performance of emulsified oil. Ag-CuO nanoparticles were synthesized via hydrothermal technique and dip-coated onto commercial membranes at varying concentrations (0.1, 0.5, and 1.0 wt.%). The prepared membranes were further examined to understand the improvements in oil-water separation due to Ag-CuO coating. All modified ceramic membranes exhibited higher hydrophilicity and decreased porosity. Additionally, the permeate flux, oil rejection, and antifouling performance of the Ag-CuO-coated membranes were more significantly improved than the pristine commercial membrane. The 0.5 wt.% modified membrane exhibited a 30% higher water flux (303.63 L m-2 h-1) and better oil rejection efficiency (97.8%) for oil/water separation among the modified membranes. After several separation cycles, the 0.5 wt.% Ag-CuO-modified membranes showed a constant permeate flux with an excellent oil rejection of >95% compared with the unmodified membrane. Moreover, the corrosion resistance of the coated membrane against acid, alkali, actual seawater, and oily wastewater was remarkable. Thus, the Ag-CuO-modified ceramic membranes are promising for oil separation applications due to their high flux, enhanced oil rejection, better antifouling characteristics, and good stability.

Rapid biosynthesis and characterization of metallic gold nanoparticles by olea europea and their potential application in photoelectrocatalytic reduction of 4-nitrophenol.

In recent years, photoelectrocatalysis of gold nanoparticles (Au NPs) has received considerable attention due to their potential to improve catalytic efficiency. Herein, ultra-small Au NPs were successfully synthesized in a single pot using olea europea leaf extract as a green reducing agent for the degradation of 4-nitrophenol. The TEM images showed uniform distribution and spherical shape of Au NPs with an average diameter of 5 nm. Taking advantage of the ability of Au nanoparticles to absorb visible and near-infrared light, 4-nitrophenol can be successfully reduced in the presence of NaBH4. Additionally, the electrochemical activity of the fabricated Au photocathode was investigated by linear sweep voltammetry in the dark and at VIS-NIR light irradiation. This showed an increased photocurrent density of 27 mA cm-2 with an onset potential of -0.71 V. This indicates that the Au photocathode is highly active at VIS-NIR light. Interestingly, the Au photocathode showed a higher current density of 37 mA cm-2 with an onset potential of -0.6 V in the presence of 4-nitrophenol during VIS-NIR irradiation, indicating that 4-nitrophenol was efficiently reduced by the photocathode. The Au photocathode completely reduced 4-nitrophenol in the wastewater within 35 min. Recyclability studies showed that the Au NPs photocathode exhibited higher stability over multiple cycles, confirming the ability of the electrode to treat wastewater over a longer period of time. This study demonstrates the effectiveness of the photoelectrochemical (PEC) process in reducing organic compounds in wastewater.

Solvent Regeneration Methods for Combined Dearomatization, Desulfurization, and Denitrogenation of Fuels Using Deep Eutectic Solvents.

Deep eutectic solvents (DESs) can be used as potential solvents for various applications. However, their recovery depends on both economic and environmental considerations. In this study, the possibilities for the recovery of methyl triphenyl phosphonium bromide/triethylene glycol (MTPPB/TEG 1:4) after the application of combined dearomatization, desulfurization, and denitrogenation of fuels are investigated. The DES was first prepared and characterized for its density, viscosity, and water content. Then, the single-stage liquid-liquid extraction was conducted in addition to testing the repetitive use of the DES. After that, two regeneration methods were studied: the stripping method (with n-heptane) and the washing method (with distilled water or diethyl ether). In addition, a parametric study was conducted to optimize the regeneration methods. The results showed that washing the used DES with distilled water was significantly more effective than stripping the DES with n-heptane. In terms of quinoline reduction, distilled water reduced the quinoline content in the DES from 3.2 to 2.1 wt %, while n-heptane showed a minor reduction in the quinoline content (3.2 to 3 wt %). It was also found that a much more effective recovery could be achieved by (i) increasing the DES-to-regeneration solvent mass ratio and (ii) increasing the number of wash cycles. Furthermore, the regeneration temperature did not have a significant effect on the recyclability of the DES. The results demonstrated that the regenerated DES was as effective in extraction as a fresh batch of DES.

Rice husk waste into various template-engineered mesoporous silica materials for different applications: A comprehensive review on recent developments.

Following the discovery of Stöber silica, the realm of morphology-controlled mesoporous silica nanomaterials like MCM-41, SBA-15, and KCC-1 has been expanded. Due to their high BET surface area, tunable pores, easiness of functionalization, and excellent thermal and chemical stability, these materials take part a vital role in the advancement of techniques and technologies for tackling the world's largest challenges in the area of water and the environment, energy storage, and biotechnology. Synthesizing these materials with excellent physicochemical properties from cost-efficient biomass wastes is a foremost model of sustainability. Particularly, SiO2 with a purity >98% can be obtained from rice husk (RH), one of the most abundant biomass wastes, and can be template engineered into various forms of mesoporous silica materials in an economic and eco-friendly way. Hence, this review initially gives insight into why to valorize RH into value-added silica materials. Then the thermal, chemical, hydrothermal, and biological methods of high-quality silica extraction from RH and the principles of synthesis of mesoporous and fibrous mesoporous silica materials like SBA-15, MCM-41, MSNs, and KCC-1 are comprehensively discussed. The potential applications of rice husk-derived mesoporous silica materials in catalysis, drug delivery, energy, adsorption, and environmental remediation are explored. Finally, the conclusion and the future outlook are briefly highlighted.