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Perfluoroalkyl substances (PFAS) are emerging contaminants present in various water sources. Their bioaccumulation and potential toxicity necessitate proper treatment to ensure safe water quality. Although iron-based monometallic photocatalysts have been reported to exhibit rapid and efficient PFAS degradation, the impact of bimetallic photocatalysts is unknown. In addition, the mechanistic effects of utilizing a support are poorly understood and solely based on physicochemical properties. This study investigates the efficacy of bimetallic photocatalysts (Fe2O3/Mn2O3) in inducing the photo-Fenton reaction for the degradation of perfluorooctane sulfonate (PFOS) and perfluorononanoic acid (PFNA) under various conditions. The rapid removal of both PFAS was observed within 10 min, with a maximum efficiency exceeding 97 % for PFOS under UV exposure, aided by the photocatalytic activation (photo-Fenton) of the oxidant (H2O2). Contrary to expectations, the use of the SiO2 support material did not significantly improve the removal efficiency. The efficacy of PFNA decreased despite SiO2 providing larger surface areas for Fe2O3/Mn2O3 loading. Further analysis revealed that the adsorption of PFAS onto the catalyst surfaces owing to electrostatic interactions contributed to the removal efficiency, where the degradation efficacy was worse than that of the catalyst with SiO2. This is because adsorption hindered the effective contact of H2O2 with catalytic reaction sites, thereby impeding the generation of hydroxyl (·OH) radicals. This study indicates the importance of considering chemical properties, including surface charge, in catalyst design to ensure effective degradation, focusing on physicochemical properties, such as surface area might overlook crucial factors.

Abstract In this study, we have demonstrated the application of sodium manganese oxide for the chemisorption of toxic acidic gases at room temperature. The fabricated alkali ceramic has Na0.4MnO2, Na2Mn3O7, and NaxMnO2 phases with a surface area of 2.6 m2 g–1. Na-Mn oxide was studied for oxidation of H2S, SO2, and NO2 gases in the concentration range of 100–500 ppm. The material exhibited a high uptake capacity of 7.13, 0.75, and 0.53 mmol g–1 for H2S, SO2, and NO2 in wet conditions, respectively. The material was reusable when regenerated simply by soaking the spent oxide in a NaOH-H2O2 solution. While the H2S chemisorption process was accompanied by sulfide, sulfur, and sulfate formation, the SO2 chemisorption process yielded only sulfate ions. The NO2 chemisorption process was accomplished by its conversion to nitrite and nitrate ions. Thus, the present work is one of the first reports on alkali ceramic utilization for room-temperature mineralization of acidic gases.

Abstract A ternary Mn–Zn–Fe oxide nanocomposite was fabricated by a one-step coprecipitation method for the remotion of H2S and SO2 gases at room temperature. The nanocomposite has ZnO, MnO2, and ferrites with a surface area of 21.03 m2 g−1. The adsorbent was effective in mineralizing acidic sulfurous gases better in wet conditions. The material exhibited a maximum H2S and SO2 removal capacity of 1.31 and 0.49 mmol g−1, respectively, in the optimized experimental conditions. The spectroscopic analyses confirmed the formation of sulfide, sulfur, and sulfite as the mineralized products of H2S. Additionally, the nanocomposite could convert SO2 to sulfate as the sole oxidation by-product. The oxidation of these toxic gases was driven by the dissolution and dissociation of gas molecules in surface adsorbed water, followed by the redox behaviour of transition metal ions in the presence of molecular oxygen and water. Thus, the study presented a potential nanocomposite adsorbent for deep desulfurization applications.

Abstract A bivalent Cu(I,II) metal–organic framework (MOF) based on the 4,4′,4″-s-Triazine-2,4,6-triyl-tribenzoate linker was synthesized via a solvothermal method. The MOF possessed 43.8% of the Cu sites as Cu+ with a surface area of 1257 m2 g−1. The detailed spectroscopic analysis confirmed dimethylformamide (DMF) solvent as the reductant responsible for Cu+ sites in the synthesized MOF. The Cu+ sites were easily accessible and prone to oxidation in hot water or acidic gas environment. The MOF showed water-induced structural change, which could be partially recovered after soaking in DMF solvent. The synthesized MOF showed a high hydrogen sulfide (H2S) uptake capacity of 4.3 mmol g–1 at 298 K and an extremely low H2S pressure of 0.0005 bar. The adsorption capacity was the highest among Cu-based MOFs with PCN-6-M being regenerable, which made it useful for deep desulfurization applications. The adsorbed H2S was mineralized to sulfide, sulfur, and sulfates, mediated by the Cu+/Cu2+ redox cycle in the presence of adsorbed water and molecular oxygen. Thus, the study confirmed that DMF as a reductant is responsible for the origin of bivalency in PCN-6-M and possibly in other Cu-based MOFs reported in the literature. Also, the developed MOF could be a potential candidate for flue gas desulfurization and gas purification applications.

Environmental issues related to phosphate and resource depletion have recently emerged as serious problems. This study focuses on solving the problems of phosphate removal and recovery using synthesized granular akaganeite (GAK). This study identified that akaganeite, which possesses an FeOOH structure in iron oxyhydroxide, can be synthesized and used as a reusable material. Immobilization with the core–shell method using polyethersulfone was applied as a strategy to recover phosphate anions from a trace of phosphate solution. GAK was successfully analyzed using SEM/TGA/BET to understand its physical properties. XRD and SAD pattern analyses suggested that the GAK powder form was amorphous in nature. The powdered akaganeite had a surface area of 231 mg2/g and a maximum adsorption capacity of 21.27 mg/g. To prevent the dispersion of powder during granulation, polyethersulfone was used as a scaffold since akaganeite particles can be effectively immobilized onto PES polymer scaffolds, as substantiated by the SEM/EDS results. Moreover, a lack of changes in the pore sizes suggested that physical properties remained unchanged. Furthermore, compared to the granular akaganeite, the surface area of powdered akaganeite decreased 4–5-fold. The adsorption kinetic of granular akaganeite fit the pseudo-second-order model. The powdered form displayed high removal efficiency, intimate with phosphate anions, when n > 1.0, instead of lower KF. On the other hand, granular akaganeite showed lower affinity when n < 1.0, but appeared positive for an adsorbate with higher KF. This implies that the granulation of akaganeite with the PES polymer did not change its adsorption property, with the maximum adsorption capacity for granular akaganeite being 3.65 mg/g.

Objectives Recently, energy-related research has shifted from developing alternative energy to the efficient management technology of the produced energy. As an alternative, research on phase change materials (PCMs) capable of absorbing and releasing heat as an energy medium has been conducted. This study developed a more efficient heat storage medium using activated carbon as a medium for the phase change material. At the same time, we developed a method for efficiently impregnating the phase change material into the activated carbon pores. Methods The activated carbon used in this experiment was charcoal powder activated carbon (250-350 mesh) and granular activated carbon. The inorganic phase change materials used in the experiment was manganese nitrate hexahydrate. The method for impregnating the phase change material was pressurization method and dilution method. The heat absorption / emission capacity of the developed material was examined within the range of 10℃ to 50℃. Results and Discussion The Scanning electron microscope (SEM) and Transmission electron microscopy energy-dispersive X-ray spectroscopy (TEM-EDX) analysis showed that the phase change material was filled in the pore of activated carbon. When the phase change material is filled by the pressurized method, the material properties of manganese nitrate hexahydrate are reflected, resulting in absorption and release of heat at each phase change temperature. As a result of experiments for the selection of the optimum solvent in the phase change material filling study using the dilution method, when ethanol was used as the solvent, the heat absorption was clearly observed even after the phase change material was loaded. As a result of selecting the optimal dilution ratio, the ratio of ethanol was determined to be 1:1 as the dilution ratio with the lowest amount of floating activated carbon. The optimal solvent removal method experimental results show that the heat absorption/release section occurred when the ethanol was removed by evaporation at 85℃ temperature. Conclusions 1) Both the pressurization method and the dilution method are filling methods in which inorganic phase change materials can be immobilized inside activated carbon, and heat absorption and release characteristics are maintained even after loading. 2) The heat absorption release was maintained for ethanol and the optimal dilution ratio was 1:1. 3) In case of the dilute solvent removal method, the heat absorption/release capacity was maintained when the solvent was removed using only the vaporization method.

Abstract Novel NaCoxOy adsorbents were fabricated by air calcination of (Na,Co)-organic frameworks at 700 °C. The NaCoxOy crystallized as hexagonal microsheets of 100–200 nm thickness with the presence of some polyhedral nanocrystals. The surface area was in the range of 1.15–1.90 m2 g−1. X-ray photoelectron spectroscopy (XPS) analysis confirmed Co2+ and Co3+ sites in MOFs, which were preserved in NaCoxOy. The synthesized adsorbents were studied for room-temperature H2S removal in both dry and moist conditions. NaCoxOy adsorbents were found ~ 80 times better than the MOF precursors. The maximum adsorption capacity of 168.2 mg g−1 was recorded for a 500 ppm H2S concentration flowing at a rate of 0.1 L min−1. The adsorption capacity decreased in the moist condition due to the competitive nature of water molecules for the H2S-binding sites. The PXRD analysis predicted Co3S4, CoSO4, Co3O4, and Co(OH)2 in the H2S-exposed sample. The XPS analysis confirmed the formation of sulfide, sulfur, and sulfate as the products of H2S oxidation at room temperature. The work reported here is the first study on the use of NaCoxOy type materials for H2S remediation.

A series of novel MnxFey@SiO2 (x,y = 1–20%) nanocomposites were synthesized for the first time via the sol-gel/combustion method with different content of precursors (Mn and Fe acetate salts). The effect of precursor content and ratio on physicochemical properties were observed by various characterization methods. Moreover, Rhodamine B (RhB) was chosen as the target pollutant to test the performance of these nanocomposites under a photocatalytic Fenton-like reaction. The results showed that the nanocomposite morphology improved by increasing Fe and Mn content. In this study, interesting behavior was observed in BET results which were different from the fact that increasing metal content can decrease the surface area. This study revealed that one metal could be more critical in controlling the properties than another. Moreover, the precursor ratio appears to have a more tangible effect on the surface area than the effect of precursor content. Among all synthesized nanocomposites, Mn1Fe5@SiO2 showed the highest surface area of 654.95 m2/g. At optimum batch conditions (temp = 25 °C, catalyst dosage = 1 g L−1, H2O2 = 75 mmolL−1, and initial RhB concentration = 50 mg L−1), complete removal (simultaneous adsorption/degradation) occurred using Mn1Fe5@SiO2 at neutral pH. This study showed that the designed nanomaterial could be used as a dual functional adsorbent/photocatalyst in different environmental applications.

In the last decades, the removal of benzene, toluene, ethylbenzene, and xylene (BTEX) has been considered a major environmental crisis. In this study, two novel nanocomposite materials (Fe2O3/SiO2 and Fe2O3-Mn2O3/SiO2) that have regeneration ability by UV irradiation have been fabricated to remove BTEX at ambient temperature. This research revealed that both nanocomposites could remove more than 85% of the BTEX in the first cycle. The adsorption capacities followed the order of ethylbenzene > m-xylene > toluene > benzene as in the molecular weight order. The reusability test using UV irradiation showed that the performance of Fe2O3/SiO2 decreased drastically after the fifth cycle for benzene. On the other hand, when Mn is located in the nanocomposite structure, Fe2O3-Mn2O3/SiO2 could maintain its adsorption performance with more than 80% removal efficiency for all the BTEX for ten consecutive cycles. The difference in the reusability of the two nanocomposites is that the electron energy (from the valence band to the conduction band) for BTEX decomposition is changed due to the presence of manganese. This study provides a promising approach for designing an economical reusable nanomaterial, which can be used for VOC-contaminated indoor air.

The influence of the electrospinning parameters on the diameter of the polyethersulfone (PES) nanofibers was demonstrated using response surface methodology. The electrospinning parameters studied were lithium chloride (LiCl) concentration, PES concentration, feed rate, and tip-to-collector distance. The average fiber diameter was correlated to these factors by using a second-order polynomial function at a 95% confidence level. The statistical analysis indicated that LiCl concentration, PES concentration, and feed rate had the significant connection with the fiber diameter, and LiCl concentration was the most important factor in determining the fiber diameter. When LiCl concentration increased, the fiber diameter decreased, because with more LiCl that is added, more applied voltage is needed to overcome the electrostatic attractions. The interactive effect between PES concentration and feed rate, the interactive effect between PES concentration and tip-to-collector distance, and the quadratic coefficients of LiCl concentration were also found to be significant. The adjusted determination coefficient (Radj2) of the model was calculated to be 0.9106. The water flux measurements showed that the decrease in the fiber diameter of the membrane caused the decrease in the initial pure water flux. The retention tests with 0.6 μm polystyrene (PS) suspension indicated that as the fiber diameter decreased, the pore sizes decreased and the particle removal efficiency increased.

Granular mesoporous silica SBA-15 (GMS) synthesized by a new and facile one step method was investigated to remove a series of pharmaceutical compounds from aqueous solutions. Characterization results obtained from TEM, XRD, and surface and porosity analyzer reveal that GMS synthesized by using inorganic and organic binder has similar pore properties with the powder-type mesoporous silica SBA-15 and does not severely reduce the Brunauer-Emmett-Teller (BET) surface area and pore volume by preventing destruction of the pores after granulation step through new synthesis method. Evaluation of GMS as an adsorbent based on adsorption kinetic, isotherm, and effect of pH shows the great adsorption capacity for selected 12 selected pharmaceuticals removal in aqueous solution. In addition, the adsorption and regeneration efficiency of GMS was maintained for given adsorption-regeneration cycles. Moreover, the column experiment to remove pharmaceuticals in industrial pharmaceutical wastewater revealed that GMS has a great potential for its real field application. [ABSTRACT FROM AUTHOR]