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Due to the increased demand for clothes by the growing population, the dye-based sectors have seen fast growth in the recent decade. Among all the dyes, methylene blue dye is the most commonly used in textiles, resulting in dye effluent contamination. It is carcinogenic, which raises the stakes for the environment. The numerous sources of methylene blue dye and their effective treatment procedures are addressed in the current review. Even among nanoparticles, photocatalytic materials, such as TiO2, ZnO, and Fe3O4, have shown greater potential for photocatalytic methylene blue degradation. Such nano-sized metal oxides are the most ideal materials for the removal of water pollutants, as these materials are related to the qualities of flexibility, simplicity, efficiency, versatility, and high surface reactivity. The use of nanoparticles generated from waste materials to remediate methylene blue is highlighted in the present review.

Persistent organic pollutants (POPs) have become a major global concern due to their large amount of utilization every year and their calcitrant nature. Due to their continuous utilization and calcitrant nature, it has led to several environmental hazards. The conventional approaches are expensive, less efficient, laborious, time-consuming, and expensive. Therefore, here in this review the authors suggest the shortcomings of conventional techniques by using nanoparticles and nanotechnology. Nanotechnology has shown immense potential for the remediation of such POPs within a short period of time with high efficiency. The present review highlights the use of nanoremediation technologies for the removal of POPs with a special focus on nanocatalysis, nanofiltration, and nanoadsorption processes. Nanoparticles such as clays, zinc oxide, iron oxide, aluminum oxide, and their composites have been used widely for the efficient remediation of POPs. Moreover, filtrations such as nanofiltration and ultrafiltration have also shown interest in the remediation of POPs from wastewater. From several pieces of literature, it has been found that nano-based techniques have shown complete removal of POPs from wastewater in comparison to conventional methods, but the cost is one of the major issues when it comes to nano- and ultrafiltration. Future research in nano-based techniques for POP remediation will solve the cost issue and will make it one of the most widely accepted and available techniques. Nano-based processes provide a sustainable solution to the problem of POPs.

One of the ideal energy carriers for the future is hydrogen. It has a high energy density and is a source of clean energy. A crucial step in the development of the hydrogen economy is the safety and affordable storage of a large amount of hydrogen. Thus, owing to its large storage capacity, good reversibility, and low cost, Magnesium hydride (MgH2) was taken into consideration. Unfortunately, MgH2 has a high desorption temperature and slow ab/desorption kinetics. Using the ball milling technique, adding cobalt lanthanum oxide (LaCoO3) to MgH2 improves its hydrogen storage performance. The results show that adding 10 wt.% LaCoO3 relatively lowers the starting hydrogen release, compared with pure MgH2 and milled MgH2. On the other hand, faster ab/desorption after the introduction of 10 wt.% LaCoO3 could be observed when compared with milled MgH2 under the same circumstances. Besides this, the apparent activation energy for MgH2–10 wt.% LaCoO3 was greatly reduced when compared with that of milled MgH2. From the X-ray diffraction analysis, it could be shown that in-situ forms of MgO, CoO, and La2O3, produced from the reactions between MgH2 and LaCoO3, play a vital role in enhancing the properties of hydrogen storage of MgH2.

The high hydrogen storage capacity (10.5 wt.%) and release of hydrogen at a moderate temperature make LiAlH4 an appealing material for hydrogen storage. However, LiAlH4 suffers from slow kinetics and irreversibility. Hence, LaCoO3 was selected as an additive to defeat the slow kinetics problems of LiAlH4. For the irreversibility part, it still required high pressure to absorb hydrogen. Thus, this study focused on the reduction of the onset desorption temperature and the quickening of the desorption kinetics of LiAlH4. Here, we report the different weight percentages of LaCoO3 mixed with LiAlH4 using the ball-milling method. Interestingly, the addition of 10 wt.% of LaCoO3 resulted in a decrease in the desorption temperature to 70 °C for the first stage and 156 °C for the second stage. In addition, at 90 °C, LiAlH4 + 10 wt.% LaCoO3 can desorb 3.37 wt.% of H2 in 80 min, which is 10 times faster than the unsubstituted samples. The activation energies values for this composite are greatly reduced to 71 kJ/mol for the first stages and 95 kJ/mol for the second stages compared to milled LiAlH4 (107 kJ/mol and 120 kJ/mol for the first two stages, respectively). The enhancement of hydrogen desorption kinetics of LiAlH4 is attributed to the in situ formation of AlCo and La or La-containing species in the presence of LaCoO3, which resulted in a reduction of the onset desorption temperature and activation energies of LiAlH4.

An alarming elevation of anthropogenic carbon dioxide (CO 2 ), primarily responsible for global warming and its drastic effects on climatic conditions, must be challenged on a priority basis. Various types of absorbents capture as much CO 2 as possible to minimize the harsh effects of environmental and climatic changes. In this study, one such compound, methyltrioctylammonium trifluoromethanesulfonate ionic liquid (IL), was analyzed experimentally and theoretically. The COSMO‐RS, a type of conductor‐like screening model, is an advanced fast method to predict the thermo‐physical properties of IL. It depends upon unimolecular, statistical thermodynamics, molecular structure, and conformation, which provides the required information for estimating interactions in ILs. The COSMO‐RS, not dependent on data, coefficients, or parameters, was used to calculate the sigma surface, profile, and potential. These parameters are crucial for predicting high‐absorbing CO 2 materials, such as ILILs. Spectroscopic methods, such as Fourier transform infrared spectroscopy (FTIR), proton nuclear magnetic resonance ( 1 H NMR), and carbon‐13 NMR ( 13 C NMR), verified the structure confirmation. In addition, spectrochemical characterization of the IL was performed using FTIR, NMR, ultraviolet–visible (UV–Vis) spectroscopy, and fluorescence. The thermal integrity of IL was measured by thermogravimetric–differential thermal analysis (TGA‐DTA) over the temperature range of 323–773 K in an oxygen ambiance with a ramp rate of 283 K/min. Due to its high potential for gas absorption, as confirmed by COSMO‐RS calculations, IL was investigated for CO 2 absorption and desorption studies at 298 K and 4.5 MPa. The maximum CO 2 absorption obtained was ~ 6.0 mmol/g, performed at similar experimental conditions. The high uptake of CO 2 might be due to fluorinated anions, as CO 2 has a high affinity for fluoroalkyl groups. According to a hysteresis‐based classification, the hysteresis formation during CO 2 absorption and desorption follows type H3, indicating the presence of both microporous and mesoporous characteristics in the sample. A detailed study of the excess Gibbs energy of sorption and the activity coefficient of the IL indicates a strong sorption capacity under moderate conditions.

In general, sludge wastewater treatments from plants are often disposed of in landfills (60%) rather than recycled, and this eventually affects the environment. Microalgae cultivation in wastewater has recently emerged as an alternate method for successfully treating wastewater in an ecofriendly way. The present study explores the possibility of growing microalgae in sludge effluent derived from industries. Industrial sludge acts as the only nutritional supplement for algal growth. The amount of organic carbon might increase the amount of protein and carbohydrates used for the production of lipids. The batch culture of different ratios of sludge wastewater was compared. The features of algal growth and biodiesel generation were studied, as well as the nitrogen and phosphate removal rates. The lipid levels of Chlorella sp. produced in this medium were clearly superior to those grown on the BG11 medium. Furthermore, this study indicated that the removal of industrial sludge and wastewater, in the absence of other nutritional supplies, allows for an efficient culture of Chlorella sp., followed by biodiesel generation. This has significant research and industrial implications since it will enable Chlorella sp. production in a mixed waste culture medium without the need for additional nutritional sources.

The intimidating level of anthropogenic CO2 in the atmosphere responsible for global warming and erratic weather conditions needs to be addressed on a priority basis. Different kinds of materials were used to capture CO2 to curtail the alarming and drastic effects of global warming. An ionic liquid (IL) 1-butyl-3-methylimidazolium methanesulfonate [C4mim][CH3SO3] was chosen, owing to its unique and efficient characteristics required for CO2 capture. Thermos-physical characteristics such as sigma surface, sigma profile, and sigma potential are calculated from the COSMO-RS model independent of any kind of experimental or coefficient data as an input. The mandatory information required for the interaction of IL with CO2 was obtained from this model. The COSMO-RS model depends upon unimolecular quantum chemical analysis associated with statistical thermodynamics, molecular structure, and conformation. The structural confirmation of [C4mim][CH3SO3] IL was performed by FTIR, 1H NMR, and 13C NMR spectroscopic methods. Spectrochemical properties are calculated by FTIR, NMR, UV-visible, and fluorescence. Maximum CO2 solubility performed at room temperature (RT) and 45 bar was found to be ~2.7 mmol/g. The uptake of CO2 indicates the presence of sulphur-functionalized anions and bulky alkyl groups in IL’s significant affinity towards CO2. According to hysteresis-based classification, CO2 sorption and desorption follows type H3 classification, which indicates the presence of microporous and mesoporous in the IL sample. The effect of functionalized anions and alkyl groups on CO2 capture is highlighted in this study. The present study is aimed at providing a detailed overview related to theoretical and experimental study and application in terms of CO2 capture of IL.

Scarcity has made fresh water too economically and socially too valuable to be used by the processing industry without restriction. Wet evaporative cooling cycles offer competitive advantages in terms of CoP compared to other cooling cycles with relatively low cost but requiring extensive quantities of water. Dry cooling, on the other hand, requires large heat-transfer areas, in addition to high power requirements. In this study, a hybrid cycle is proposed for high-end cooling loads of 215 MW. The proposed cycle combines the benefits of phase change to make dry cycles competitive. Furthermore, the proposed cycle also diminishes the extensive use of various chemicals used in wet cooling cycles. The applicable dry bulb temperature range is 25–50 °C. Variations in cooling fluid cold temperature due to ambient conditions are curtailed to a maximum of 2 °C by the proposed cycle. A technoeconomic comparison of the proposed solution to wet evaporative cooling is presented, and the effects are summarized without providing extensive design calculations. ASPEN modules are used design and simulation.

Nanocrystalline aluminum-doped manganese ferrite was synthesized by facile thermal treatment method. Nanostructure-doped ferrite with crystalline size that ranged between 3.71 and 6.35 nm was characterized via X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and vibrating-sample magnetometry (VSM). The Scherrer and Williamson-Hall hypothesis techniques were utilized to determine lattice constants and strain. Various types of structural properties including octahedral and tetrahedral site radius, bond lengths and angles, hopping parameter, oxygen positional parameters, site bonds, and edge lengths were determined from XRD spectrum analysis. Discrepancy in the hypothetically expected angle indicates improvement of A-B superexchange intercommunication. Furthermore, magnetic-hysteresis (M-H) and XPS analysis support the claim of enhancement. The presence of the ionic nature of iron and manganese in ferrite is FeII, FeIII, MnII, and MnIV as revealed by the results of XPS. Moreover, XPS assists in an excellent way to understand the properties such as configuration, chemical nature, and average inversion degree of doped ferrite samples. The spin noncollinearity and exquisite interaction amid the sublattice are responsible for the decrease in the saturation and remnant magnetization determined from the hysteresis loop at ambient temperature with maximum magnetic field of 1.8 T.

Different wounds take a while to heal, and the process is frequently accompanied by bacterial infection and scar formation. This study aimed to fabricate polyurethane (PU) fibers through electrospinning, utilizing a mixture of THF and DMF solvents in a 90:10 ratio. Subsequently, these fibers were coated with different concentrations of hyaluronic acid (HA) and silver (Ag) nanoparticles (NPs) using the hydrothermal treatment to create biocompatible and antibacterial scaffolds applicable to wound management. Pristine samples served as a basis for comparison. Following high-temperature usage during the hydrothermal coating, the Field emission scanning electron microscopy (FE-SEM) results showed defect-free morphology. However, the fibers’ diameter significantly increased by layer of HA. In particular, the diameter of the PU fibers was 1.87 ± 1.1 µm, whereas the fibers with the maximum amount of HA (0.5%) had an enlargement of 4.43 ± 1.4 µm in fiber diameter. The Fourier transform infrared (FTIR) spectroscopy demonstrated the presence of distinctive functional groups, supporting the hypothesis that HA and Ag NPs were efficaciously coated on PU fibers. Moreover, HA-coated fibers improved hydrophilicity, mechanical strength, thermal stability, degradability, and biomineralization. Notably, the Ag-coated scaffolds exhibited antibacterial activity against E. coli and S. aureus. The MTT assay, DAPI staining, and FE-SEM results after culturing HEK 293T cells have demonstrated the biocompatibility of the nanocomposite fibers. In other words, the developed HA and Ag NPs coated PU fibers by hydrothermal technique would be a futuristic method for promoting tissue healing and imparting antibacterial ability in curing skin wounds.