Advanced oxidation and biological integrated processes for pharmaceutical wastewater treatment: A review.

The stress of pharmaceutical and personal care products (PPCPs) discharging to water bodies and the environment due to increased industrialization has reduced the availability of clean water. This poses a potential health hazard to animals and human life because water contamination is a great issue to the climate, plants, humans, and aquatic habitats. Pharmaceutical compounds are quantified in concentrations ranging from ng/Lto µg/L in aquatic environments worldwide. According to (Alsubih et al., 2022), the concentrations of carbamazepine, sulfamethoxazole, Lutvastatin, ciprofloxacin, and lorazepam were 616-906 ng/L, 16,532-21635 ng/L, 694-2068 ng/L, 734-1178 ng/L, and 2742-3775 ng/L respectively. Protecting and preserving our environment must be well-driven by all sectors to sustain development. Various methods have been utilized to eliminate the emerging pollutants, such as adsorption and biological and advanced oxidation processes. These methods have their benefits and drawbacks in the removal of pharmaceuticals. Successful wastewater treatment can save the water bodies; integrating green initiatives into the main purposes of actor firms, combined with continually periodic awareness of the current and potential implications of environmental/water pollution, will play a major role in water conservation. This article reviews key publications on the adsorption, biological, and advanced oxidation processes used to remove pharmaceutical products from the aquatic environment. It also sheds light on the pharmaceutical adsorption capability of adsorption, biological and advanced oxidation methods, and their efficacy in pharmaceutical concentration removal. A research gap has been identified for researchers to explore in order to eliminate the problem associated with pharmaceutical wastes. Therefore, future study should focus on combining advanced oxidation and adsorption processes for an excellent way to eliminate pharmaceutical products, even at low concentrations. Biological processes should focus on ideal circumstances and microbial processes that enable the simultaneous removal of pharmaceutical compounds and the effects of diverse environments on removal efficiency.

Production of hydrogen using plastic waste via Aspen Hysys simulation.

Plastic waste is being manufactured for the production of hydrogen. The amount of plastic waste collected annually is 189,953 tonnes from adjacent nations like Indonesia and Malaysia. Polyethylene (PE), Polypropylene (PP), Polyethylene Terephthalate (PET), Polyvinyl chloride (PVC), and Polystyrene (PS) are the five most prevalent forms of plastic found in most waste. Pyrolysis, water gas shift and steam reforming reaction, and pressure swing adsorption are the three main phases utilized and studied. In this research, authors examines the energy consumption on every stage. The plastic waste can be utilized to manufacture many hydrocarbons using the pyrolysis reaction. For this process, fast pyrolysis is being used at a temperature of 500 °C. A neutralization process is also needed due to the presence of Hydrochloric acid from the pyrolysis reaction, with the addition of sodium hydroxide. This is being carried to prevent any damage to the reactor during the process. Secondly, the steam reforming process continues after the water gas shift reaction has produced steam and carbon monoxide, followed by carbon dioxide and hydrogen formation. Lastly, pressure swing adsorption is designed to extract H2S and CO2 from the water gas shift and steam reforming reaction for greater purity of hydrogen. From the simulation study, it is observed that using various types of plastic waste procured (total input of 20,000 kg per hour of plastics) from, Brunei Darussalam, Malaysia and Indonesia, can produce about 340,000 tons of Hydrogen per year. Additionally, the annual profit of the Hydrogen production is estimated to be between $ 271,158,100 and $ 358,480,200. As per the economic analysis, it can be said that its a good to start hydrogen production plant in these regions.

Exploring the impact of defect energy levels in CdTe/Si dual-junction solar cells using wxAMPS.

A numerical analysis of a CdTe/Si dual-junction solar cell in terms of defect density introduced at various defect energy levels in the absorber layer is provided. The impact of defect concentration is analyzed against the thickness of the CdTe layer, and variation of the top and bottom cell bandgaps is studied. The results show that CdTe thin film with defects density between 1014 and 1015 cm-3 is acceptable for the top cell of the designed dual-junction solar cell. The variations of the defect concentrations against the thickness of the CdTe layer indicate that the open circuit voltage, short circuit current density, and efficiency (ƞ) are more affected by the defect density at higher CdTe thickness. In contrast, the Fill factor is mainly affected by the defect density, regardless of the thin film's thickness. An acceptable defect density of up to 1015 cm-3 at a CdTe thickness of 300 nm was obtained from this work. The bandgap variation shows optimal results for a CdTe with bandgaps ranging from 1.45 to 1.7 eV in tandem with a Si bandgap of about 1.1 eV. This study highlights the significance of tailoring defect density at different energy levels to realize viable CdTe/Si dual junction tandem solar cells. It also demonstrates how the impact of defect concentration changes with the thickness of the solar cell absorber layer.

Insights into kinetics, thermodynamics, and mechanisms of chemically activated sunflower stem biochar for removal of phenol and bisphenol-A from wastewater.

This study synthesized a highly efficient KOH-treated sunflower stem activated carbon (KOH-SSAC) using a two-step pyrolysis process and chemical activation using KOH. The resulting material exhibited exceptional properties, such as a high specific surface area (452 m2/g) and excellent adsorption capacities for phenol (333.03 mg/g) and bisphenol A (BPA) (365.81 mg/g). The adsorption process was spontaneous and exothermic, benefiting from the synergistic effects of hydrogen bonding, electrostatic attraction, and stacking interactions. Comparative analysis also showed that KOH-SSAC performed approximately twice as well as sunflower stem biochar (SSB), indicating its potential for water treatment and pollutant removal applications. The study suggests the exploration of optimization strategies to further enhance the efficiency of KOH-SSAC in large-scale scenarios. These findings contribute to the development of improved materials for efficient water treatment and pollution control.

Bo-derived waste neem to enriching reinforced hybrid composite for environmental remediation.

The utilization of natural fibres often entails a lesser environmental impact when compared to synthetic fibres. Biodegradable natural fibres minimize waste and pollution, and promote sustainability, but their weaker bonds limit their resilience. These issues can be addressed by customizing the composite's mechanical properties with natural and synthetic fibres. In this study, hybrid composites were created using the hand layup method with a novel dissimilar layer arrangement of neem (N), sisal (S), and glass (G) fibre and analyze its mechanical and thermal properties. Experimental observation shows that the GN composite had a higher maximum ultimate tensile strength of 26 N/mm2 than the GS, GNS, and GSN composites. The GN composite had a percentage elongation of 6.33%, similar to the percentage elongation of the GS composite (6.833%), and it also had a higher ultimate shear strength of 50 MPa. The composite GS absorbed 6.6 J energy, higher than the composites GN, GNS, and GNS, which absorbed 6.1 J, 4.5 J, and 4.5 J, respectively. The fractured surface's SEM images were obtained and analyzed for failure. The results demonstrated that the hybridization was effective, and better properties can be obtained by combining neem, sisal, and glass fiber, and it can be used for other requirements, including strength, weight, cost, and ecological impact.

Rapid adsorptive removal of eosin yellow and methyl orange using zeolite Y.

In this study, zeolite Y was synthesised using a novel method. The heat generated from the reaction of H2SO4 with metakaolin was used as a heat source instead of applying external heat for the dealuminated process. The synthesised zeolite Y produced was analysed by scanning electron microscope (SEM), X-ray diffraction (XRD), Fourier-infrared spectroscopy (FTIR), energy dispersive X-ray spectroscopy (EDS) and Brunauer-Emmett-Teller (BET). Zeolite Y synthesis was mesoporous because of its pore diameter (30.53 nm), as shown in the BET results. Surface area and pore size decrease after adsorption due to dye deposition on the adsorbent's surface. FTIR has bonds like O-H, C-H, -CH3, and -COOH responsible for adsorption. The maximum adsorption capacity of eosin yellow (EY) and methyl orange (MO) on to zeolite Y by the Langmuir isotherm was 52.91 mg/g and 20.62 mg/g respectively, at pH 2.5 and 8 for EY and MO dye. The batch adsorption studies were conducted, and the influence of different parameters (i.e., adsorbent dose, adsorption time, initial dye concentration, pH and temperature) was investigated. Experimental data were analysed by two linear model equations (Langmuir and Freundlich isotherms), and it was found that the Langmuir isotherm model best describes the adsorption data for methyl orange and Freundlich isotherm for eosin yellow, respectively. Adsorption rate constants were determined using linear pseudo-first-order and pseudo-second-order. The results showed that MO and EY dye adsorption onto zeolite Y followed a pseudo-second-order kinetic model. Thermodynamic studies show that adsorption was an exothermic reaction (enthalpy < 0) and feasible ([Formula: see text]) at various temperatures under investigation.

Insights into isotherms, kinetics, and thermodynamics of adsorption of acid blue 113 from an aqueous solution of nutraceutical industrial fennel seed spent.

Research studies have been carried out to accentuate Fennel Seed Spent, a by-product of the Nutraceutical Industry, as an inexpensive, recyclable and operational biosorbent for bioremediation of Acid Blue 113 (AB113) in simulated water-dye samples and textile industrial effluent (TIE). The physical process of adhesion of AB113 on the surface of the biosorbent depends on various parameters, such as the initial amount of the dye, amount and expanse of the biosorbent particles, pH of the solution and temperature of the medium. The data obtained was analyzed using three two-parameter and five three-parameter adsorption isotherm models to glean the adsorbent affinities and interaction mechanism of the adsorbate molecules and adsorbent surface. The adsorption feature study is conducted employing models of Weber-Morris, pseudo 1st and 2nd order, diffusion film model, Dumwald-Wagner and Avrami model. The study through 2nd order pseudo and Avrami models produced complementary results for the authentication of experimental data. The thermodynamic features, ΔG0, ΔH0, and ΔS0 of the adsorption process are acclaimed to be almost spontaneous, physical in nature and endothermic in their manifestation. Surface characterization was carried out using Scanner Electron Microscopy, and identification and determination of chemical species and molecular structure was performed using Infrared Spectroscopy (IR). Maximum adsorption evaluated using statistical optimization with different combinations of five independent variables to study the individual as well as combined effects by Fractional Factorial Experimental Design (FFED) was 236.18 mg g-1 under optimized conditions; pH of 2, adsorbent dosage of 0.500 g L-1, and an initial dye concentration of 209.47 mg L-1 for an adsorption time of 126.62 min with orbital shaking of 165 rpm at temperature 49.95 °C.

Experimental and numerical assessment of the flexural response of banana fiber sandwich epoxy composite.

Recently, most service or product-oriented industries have been focusing on their activities to uphold the green and sustainable environment protocol owing to the increased environmental pollution. Concerning this issue, industries are now concentrating on developing recyclable or waste materials products. This research advocates developing and validating a banana fiber sandwich composite to promote the beneficial usage of bio-waste. The composite sandwich specimens were fabricated with resin-impregnated woven banana fiber mat as a skin, and the core was reinforced with three different weight percentages (5, 7.5 and 10%) of chopped banana fiber. The sandwich specimens were pressed into a three-point bending test to validate the structural integrity. The flexural characteristics like flexural strength and modulus were examined experimentally, whereas the key strength indices like flexural stiffness and core shear modulus were evaluated analytically. Post-fracture surfaces were studied through a scanning electron microscope to investigate the failure mechanism. The experimental and analytical results indicate that 10% banana fiber content in the sandwich core increases the flexural strength and flexural modulus to 225% and 147%, respectively, compared to the neat epoxy core. The numerical simulation was also performed through FEA to validate the experimental findings. The numerical results are in good concurrence with the experimental one.

A state-of-art-review on emerging contaminants: Environmental chemistry, health effect, and modern treatment methods.

Pollution problems are increasingly becoming e a priority issue from both scientific and technological points of view. The dispersion and frequency of pollutants in the environment are on the rise, leading to the emergence have been increasing, including of a new class of contaminants that not only impact the environment but also pose risks to people's health. Therefore, developing new methods for identifying and quantifying these pollutants classified as emerging contaminants is imperative. These methods enable regulatory actions that effectively minimize their adverse effects to take steps to regulate and reduce their impact. On the other hand, these new contaminants represent a challenge for current technologies to be adapted to control and remove emerging contaminants and involve innovative, eco-friendly, and sustainable remediation technologies. There is a vast amount of information collected in this review on emerging pollutants, comparing the identification and quantification methods, the technologies applied for their control and remediation, and the policies and regulations necessary for their operation and application. In addition, This review will deal with different aspects of emerging contaminants, their origin, nature, detection, and treatment concerning water and wastewater.

Sustainable approach for catalytic green epoxidation of oleic acid with applied ion exchange resin.

Epoxides were primarily derived from petroleum-based sources. However, there has been limited research on optimizing the process parameters for epoxidized palm oil-derived oleic acid, resulting in its underutilization. Therefore, this study aimed to optimize the catalytic epoxidation of palm oleic acid concerning the oxirane content by applying ion exchange resin as a catalyst. Epoxidized oleic acid was produced using in-situ-formed performic acid by combining formic acid as the oxygen carrier with hydrogen peroxide as the oxygen donor. The findings revealed that the optimal reaction conditions for producing epoxidized oleic acid with the highest oxirane content were an Amberlite IR-120 catalyst loading of 0.9 g, a molar ratio of formic acid to oleic acid of 1:1., and a molar ratio of hydrogen peroxide to oleic acid of 1:1.1. By employing these optimal conditions, the maximum relative conversion of palm oleic acid to oxirane was achieved at 85%. The reaction rate constants (k) based on the optimized epoxidized oleic acid are determined as follows: k11 = 20 mol L-1 min-1, k12 = 2 mol L-1 min-1, and k2 = 20 mol L-1 min-1. The findings validated the kinetic model by showing good agreement between the simulation and experimental data.

Development of sustainable biomass residues for biofuels applications.

A comprehensive understanding of physiochemical properties, thermal degradation behavior and chemical composition is significant for biomass residues before their thermochemical conversion for energy production. In this investigation, teff straw (TS), coffee husk (CH), corn cob (CC), and sweet sorghum stalk (SSS) residues were characterized to assess their potential applications as value-added bioenergy and chemical products. The thermal degradation behavior of CC, CH, TS and SSS samples is calculated using four different heating rates. The activation energy values ranged from 81.919 to 262.238 and 85.737-212.349 kJ mol-1 and were generated by the KAS and FWO models and aided in understanding the biomass conversion process into bio-products. The cellulose, hemicellulose, and lignin contents of CC, CH, TS, and SSS were found to be in the ranges of 31.56-41.15%, 23.9-32.02%, and 19.85-25.07%, respectively. The calorific values of the residues ranged from 17.3 to 19.7 MJ/kg, comparable to crude biomass. Scanning electron micrographs revealed agglomerated, irregular, and rough textures, with parallel lines providing nutrient and water transport pathways in all biomass samples. Energy Dispersive X-ray spectra and X-ray diffraction analysis indicated the presence of high carbonaceous material and crystalline nature. FTIR analysis identified prominent band peaks at specific wave numbers. Based on these findings, it can be concluded that these residues hold potential as energy sources for various applications, such as the textile, plastics, paints, automobile, and food additive industries.

Adsorptive removal of acid red 18 dye from aqueous solution using hexadecyl-trimethyl ammonium chloride modified nano-pumice.

Discharging untreated dye-containing wastewater gives rise to environmental pollution. The present study investigated the removal efficiency and adsorption mechanism of Acid Red 18 (AR18) utilizing hexadecyl-trimethyl ammonium chloride (HDTMA.Cl) modified Nano-pumice (HMNP), which is a novel adsorbent for AR18 removal. The HDTMA.Cl is characterized by XRD, XRF, FESEM, TEM, BET and FTIR analysis. pH, contact time, initial concentration of dye and adsorbent dose were the four different parameters for investigating their effects on the adsorption process. Response surface methodology-central composite design was used to model and improve the study to reduce expenses and the number of experiments. According to the findings, at the ideal conditions (pH = 4.5, sorbent dosage = 2.375 g/l, AR18 concentration = 25 mg/l, and contact time = 70 min), the maximum removal effectiveness was 99%. The Langmuir (R2 = 0.996) and pseudo-second-order (R2 = 0.999) models were obeyed by the adsorption isotherm and kinetic, respectively. The nature of HMNP was discovered to be spontaneous, and thermodynamic investigations revealed that the AR18 adsorption process is endothermic. By tracking the adsorption capacity of the adsorbent for five cycles under ideal conditions, the reusability of HMNP was examined, which showed a reduction in HMNP's adsorption effectiveness from 99 to 85% after five consecutive recycles.

Light-absorption-driven photocatalysis and antimicrobial potential of PVP-capped zinc oxide nanoparticles.

Toxic dyes in water bodies and bacterial pathogens pose serious global challenges to human health and the environment. Zinc oxide nanoparticles (ZnO NPs) demonstrate remarkable photocatalytic and antibacterial potency against reactive dyes and bacterial strains. In this work, PVP-ZnO NPs have been prepared via the co-precipitation method using polyvinylpyrrolidone (PVP) as a surfactant. The NPs' microstructure and morphology were studied using X-ray diffraction (XRD), having a size of 22.13 nm. High-resolution transmission electron microscope (HR-TEM) and field emission scanning electron microscopy (FESEM) analysis showed spherical-shaped PVP-ZnO NPs with sizer ranging from 20 to 30 nm. Fourier Transform Infrared Spectroscopy (FT-IR) confirmed the hybrid nature of the NPs, and UV-Vis spectroscopy showed an absorption peak at 367 nm. The PVP-ZnO NPs exhibited high photocatalytic activity, achieving 88% and nearly 95% degradation of reactive red-141 azo dye with 10 mg and 20 mg catalyst dosages, respectively. The antibacterial properties of the NPs were demonstrated against Escherichia coli and Bacillus subtilis, with inhibition zones of 24 mm and 20 mm, respectively. These findings suggest that PVP-ZnO NPs can be effectively used for water treatment, targeting both dye and pathogenic contaminants.

Cellulose microcrystalline: A promising ecofriendly approach to control Culex quinquefasciatus larvae.

The growing use of synthetic chemical compounds/substances in vector control of mosquitoes, associated with their adverse effects on the environment and non-target organisms, has demanded the development of eco-friendly alternatives. In this context, this study aimed to evaluate the larvicidal action of different cellulose microcrystalline (CMs) concentrations and investigate their toxicity mechanisms in Culex quinquefasciatus fourth instar larvae as a model species. Probit analysis revealed that the median lethal concentrations (LC50) for 24 h and 36 h exposure were 100 and 58.29 mg/L, respectively. We also showed that such concentrations induced a redox imbalance in the larvae, marked by an increase in the production of reactive oxygen species (ROS) and thiobarbituric acid reactive substances (TBARS), as well as a reduction in the activity of superoxide dismutase (SOD) and catalase (CAT). Furthermore, different alterations in the external morphology of the larvae were associated with the ingestion of CMs. On the other hand, exposure of adult zebrafish (Danio rerio) to LC5024h and LC5036h for seven days did not induce any behavioral changes or alterations mutagenic, genotoxic, biochemical, or in the production of cytokines IFN-γ and IL-10. Thus, taken together, our study demonstrates for the first time that the use of CMs can constitute a promising strategy in the control of C. quinquefasciatus larvae, combining insecticidal efficiency with an "eco-friendly" approach in the fight against an important mosquito vector of several human diseases.

Investigating the Correlation between Electrolyte Concentration and Electrochemical Properties of Ionogels.

Ionogels are hybrid materials comprising an ionic liquid confined within a polymer matrix. They have garnered significant interest due to their unique properties, such as high ionic conductivity, mechanical stability, and wide electrochemical stability. These properties make ionogels suitable for various applications, including energy storage devices, sensors, and solar cells. However, optimizing the electrochemical performance of ionogels remains a challenge, as the relationship between specific capacitance, ionic conductivity, and electrolyte solution concentration is yet to be fully understood. In this study, we investigate the impact of electrolyte solution concentration on the electrochemical properties of ionogels to identify the correlation for enhanced performance. Our findings demonstrate a clear relationship between the specific capacitance and ionic conductivity of ionogels, which depends on the availability of mobile ions. The reduced number of ions at low electrolyte solution concentrations leads to decreased ionic conductivity and specific capacitance due to the scarcity of a double layer, constraining charge storage capacity. However, at a 31 vol% electrolyte solution concentration, an ample quantity of ions becomes accessible, resulting in increased ionic conductivity and specific capacitance, reaching maximum values of 58 ± 1.48 µS/cm and 45.74 F/g, respectively. Furthermore, the synthesized ionogel demonstrates a wide electrochemical stability of 3.5 V, enabling diverse practical applications. This study provides valuable insights into determining the optimal electrolyte solution concentration for enhancing ionogel electrochemical performance for energy applications. It highlights the impact of ion pairs and aggregates on ion mobility within ionogels, subsequently affecting their resultant electrochemical properties.

A comparative study on characteristics of composite (Cr3C2-NiCr) clad developed through diode laser and microwave energy.

A typical ferrite/martensitic heat-resistant steel (T91) is widely used in reheaters, superheaters and power stations. Cr3C2-NiCr-based composite coatings are known for wear-resistant coatings at elevated temperature applications. The current work compares the microstructural studies of 75 wt% Cr3C2- 25 wt% NiCr-based composite clads developed through laser and microwave energy on a T91 steel substrate. The developed clads of both processes were characterized through a field emission scanning electron microscope (FE-SEM) attached with energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD) and assessment of Vickers microhardness. The Cr3C2-NiCr based clads of both processes revealed better metallurgical bonding with the chosen substrate. The microstructure of the developed laser clad shows a distinctive dense solidified structure, with a rich Ni phase occupying interdendritic spaces. In the case of microwave clad, the hard chromium carbide particles consistently dispersed within the soft nickel matrix. EDS study evidenced that the cell boundaries are lined with chromium where Fe and Ni were found inside the cells. The X-ray phase analysis of both the processes evidenced the common presence of phases like chromium carbides (Cr7C3, Cr3C2, Cr23C6), Iron Nickel (FeNi3) and chromium-nickel (Cr3Ni2, CrNi), despite these phases iron carbides (Fe7C3) are observed in the developed microwave clads. The homogeneous distributions of such carbides in the developed clad structure of both processes indicated higher hardness. The typical microhardness of the laser-clad (1142 ± 65HV) was about 22% higher than the microwave clad (940 ± 42 HV). Using a ball-on-plate test, the study analyzed microwave and laser-clad samples' wear behavior. Laser-cladding samples showed superior wear resistance due to hard carbide elements. At the same time, microwave-clad samples experienced more surface damage and material loss due to micro-cutting, loosening, and fatigue-induced fracture.

Experimental investigation on a solar parabolic collector using water-based multi-walled carbon-nanotube with low volume concentrations.

A limited experimental work was on multi-walled carbon nanotube (MWCNT)-water nanofluid with surfactant in the solar parabolic collector at low volume concentrations. At high-volume concentrated nanofluid, the pressure drop was more due to an increase in the viscosity of the working fluid and an increase in the nanoparticle cost; hence it is not economical. This report attempted to use Sodium Dodecyl Benzene Sulfonate (SDBS) surfactant in the low-volume concentrated MWCNT-water nanofluid to establish effective heat transfer in solar parabolic collector applications. The stable MWCNT-water nanofluid was prepared at 0.0158, 0.0238, and 0.0317 volume concentrations. The experiments were conducted from 10:00 to 16:00 at 6, 6.5 and 7 L/min flow rates concerning ASHRAE Standards. At the 7 L/min flow rate of the working fluid, having a minimum temperature difference between the working fluid and absorber tube leads to better heat transfer. The increased volume concentration of MWCNT in the water enhances the surface area interaction between water and MWCNT nanoparticles. This results in maximum solar parabolic collector efficiency at 0.0317 vol% with a 7 L/min flow rate and 10-11% higher than the distilled water.

A review of novel green adsorbents as a sustainable alternative for the remediation of chromium (VI) from water environments.

The presence of heavy metal, chromium (VI), in water environments leads to various diseases in humans, such as cancer, lung tumors, and allergies. This review comparatively examines the use of several adsorbents, such as biosorbents, activated carbon, nanocomposites, and polyaniline (PANI), in terms of the operational parameters (initial chromium (VI) concentration (Co), temperature (T), pH, contact time (t), and adsorbent dosage) to achieve the Langmuir's maximum adsorption capacity (qm) for chromium (VI) adsorption. The study finds that the use of biosorbents (fruit bio-composite, fungus, leave, and oak bark char), activated carbons (HCl-treated dry fruit waste, polyethyleneimine (PEI) and potassium hydroxide (KOH) PEI-KOH alkali-treated rice waste-derived biochar, and KOH/hydrochloric acid (HCl) acid/base-treated commercial), iron-based nanocomposites, magnetic manganese-multiwalled carbon nanotubes nanocomposites, copper-based nanocomposites, graphene oxide functionalized amino acid, and PANI functionalized transition metal are effective in achieving high Langmuir's maximum adsorption capacity (qm) for chromium (VI) adsorption, and that operational parameters such as initial concentration, temperature, pH, contact time, and adsorbent dosage significantly affect the Langmuir's maximum adsorption capacity (qm). Magnetic graphene oxide functionalized amino acid showed the highest experimental and pseudo-second-order kinetic model equilibrium adsorption capacities. The iron oxide functionalized calcium carbonate (IO@CaCO3) nanocomposites showed the highest heterogeneous adsorption capacity. Additionally, Syzygium cumini bark biosorbent is highly effective in treating tannery industrial wastewater with high levels of chromium (VI).

Performance analysis of biofuel-ethanol blends in diesel engine and its validation with computational fluid dynamics.

The engine tests aimed to produce comparable data for fuel consumption, exhaust emissions, and thermal efficiency. The computational fluid dynamics (CFD) program FLUENT was used to simulate the combustion parameters of a direct injection diesel engine. In-cylinder turbulence is controlled using the RNG k-model. The model's conclusions are validated when the projected p-curve is compared to the observed p-curve. The thermal efficiency of the 50E50B blend (50% ethanol, 50% biofuel) is higher than the other blends as well as diesel. Diesel has lower brake thermal efficiency among the other fuel blends used. The 10E90B mix (10% ethanol, 90% biofuel) has a lower brake-specific fuel consumption (BSFC) than other blends but is slightly higher than diesel. The temperature of the exhaust gas rises for all mixtures as the brake power is increased. CO emissions from 50E50B are lower than diesel at low loads but slightly greater at heavy loads. According to the emission graphs, the 50E50B blend produces less HC than diesel. NOx emission rises with increasing load in the exhaust parameter for all mixes. A 50E50B biofuel-ethanol combination achieves the highest brake thermal efficiency, 33.59%. The BSFC for diesel is 0.254 kg/kW-hr at maximum load, while the BSFC for the 10E90B mix is 0.269 kg/kW-hr, higher than diesel. In comparison to diesel, BSFC has increased by 5.90%.