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The ecosystem and human health are both significantly affected by the occurrence of potentially harmful heavy metals in the aquatic environment. In general, wastewater comprises an array of heavy metals, and the existence of other competing heavy metal ions might affect the adsorptive elimination of one heavy metal ion. Therefore, to fully comprehend the adsorbent's efficiency and practical applications, the abatement of heavy metals in multicomponent systems is important. In the current study, the multicomponent adsorption of heavy metals from different complex mixtures, such as binary, ternary, quaternary, and quinary solutions, utilizing various adsorbents are reviewed in detail. According to the systematic review, the adsorbents made from locally and naturally occurring materials, such as biomass, feedstocks, and industrial and agricultural waste, are effective and promising in removing heavy metals from complex water systems. The systematic study further discovered that numerous studies evaluate the adsorption characteristics of an adsorbent in a multicomponent system using various important independent adsorption parameters. These independent adsorption parameters include reaction time, solution pH, agitation speed, adsorbent dosage, initial metal ion concentration, ionic strength as well as reaction temperature, which were found to significantly affect the multicomponent sorption of heavy metals. Furthermore, through the application of the multicomponent adsorption isotherms, the competitive heavy metals sorption mechanisms were identified and characterized by three primary kinds of interactive effects including synergism, antagonism, and non-interaction. Despite the enormous amount of research and extensive data on the capability of different adsorbents, several significant drawbacks hinder adsorbents from being used practically and economically to remove heavy metal ions from multicomponent systems. As a result, the current systematic review provides insights and perspectives for further studies through the thorough and reliable analysis of the relevant literature on heavy metals removal from multicomponent systems.
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This article presents detailed structural, electronic, magnetic, and thermoelectric properties of two experimentally existing isostructural variant perovskite compounds Tl2 NbX6 (X = Cl, Br) with the help of first principles calculations. As per requirement of stability in the device applications, the structural and thermodynamic stabilities were, respectively verified by tolerance factor and negative formation energies. The structural parameters in ferromagnetic phase were calculated and found in close agreement with the available experimental results. The electronic nature was found as half metallic from spin polarized calculations of electronic band structures and density of states, where the semiconductor nature was found in the spin down states and metallic nature in the spin up states. The magnetic moments of both the compounds were calculated as 1 µB majorly contributed by Nb atom. The Boltzmann transport theory was implemented via BoltzTraP for calculating the spin resolved thermoelectric parameters, such as Seebeck coefficient, electronic and thermal conductivities, and figure of merit. Overall, both the compounds were found suitable for use in spintronics and spin Seebeck effect for energy applications.
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The selective electrochemical reduction of oxygen (O2) via 3e- pathway for the production of hydroxyl radicals (HO) is a promising alternative to conventional electro-Fenton process. Here, we developed a nitrogen-doped CNT-encapsulated Ni nanoparticle electrocatalyst (Ni@N-CNT) with high O2 reduction selectivity for the generation of HOâ¢via 3e- pathway. Exposed graphitized N on the CNT shell, and Ni nanoparticles encapsulated within the tip of the N-CNT, played a key role in the generation of H2O2 intermediate (*HOOH) via a 2e- oxygen reduction reaction. Meanwhile, those encapsulated Ni nanoparticles at the tip of the N-CNT facilitated the sequential HO⢠generation by directly decomposing the electrogenerated *H2O2 in a 1e- reduction reaction on the N-CNT shell without inducing Fenton reaction. Improved bisphenol A (BPA) degradation efficiency were observed when compared with conventional batch system (97.5% vs 66.4%). Trials using Ni@N-CNT in a flow-through configuration demonstrated a complete removal of BPA within 30 min (k = 0.12 min-1) with a limited energy consumption of 0.068 kW·h·g-1 TOC.
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There are several environmental and human health impacts if human hair waste is not adequately disposed of. In this study, pyrolysis of discarded human hair was carried out. This research focused on the pyrolysis of discarded human hair under controlled environmental conditions. The effects of the mass of discarded human hair and temperature on bio-oil yield were studied. The proximate and ultimate analyses and calorific values of disposed of human hair, bio-oil, and biochar were determined. Further, chemical compounds of bio-oil were analyzed using a gas chromatograph and a mass spectrometer. Finally, the kinetic modeling and behavior of the pyrolysis process were characterized through FT-IR spectroscopy and thermal analysis. Based on the optimized mass of disposed of human hair, 250 g had a better bio-oil yield of 97% in the temperature range of 210-300 °C. The different parameters of bio-oil were: pH (2.87), specific gravity (1.17), moisture content (19%), heating value (19.34 MJ/kg), and viscosity (50 CP). C (56.4%), H (6.1%), N (0.16%), S (0.01%), O (38.4%), and Ash (0.1%) were discovered to be the elemental chemical composition of bio-oil (on a dry basis). During breakdown, the release of different compounds like hydrocarbons, aldehydes, ketones, acids, and alcohols takes place. According to the GC-MS results, several amino acids were discovered in the bio-oil, 12 abundant in the discarded human hair. The FTIR and thermal analysis found different concluding temperatures and wave numbers for functional groups. Two main stages are partially separated at about 305 °C, with maximum degradation rates at about 293 oC and 400-4140 °C, respectively. The mass loss was 30% at 293 0C and 82% at temperatures above 293 0C. When the temperature reached 4100C, the entire bio-oil from discarded human hair was distilled or thermally decomposed.
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Contamination of water resources by industrial effluents containing heavy metal ions and management of solid waste from agricultural and food industries is a serious issue. This study presents the valorization of waste walnut shells as an effective and environment-friendly biosorbent for sequestrating Cr(VI) from aqueous media. The native walnut shell powder (NWP) was chemically modified with alkali (AWP) and citric acid (CWP) to obtain modified biosorbents with abundant availability of pores as active centers, as confirmed by BET analysis. During batch adsorption studies, the process parameters for Cr(VI) adsorption were optimized at pH 2.0. The adsorption data were fitted to isotherm and kinetic models to compute various adsorption parameters. The adsorption pattern of Cr(VI) was well explained by the Langmuir model suggesting the adsorbate monolayer formation on the surface of the biosorbents. The maximum adsorption capacity, qm, for Cr(VI) was achieved for CWP (75.26 mg/g), followed by AWP (69.56 mg/g) and NWP (64.82 mg/g). Treatment with sodium hydroxide and citric acid improved the adsorption efficiency of the biosorbent by 4.5 and 8.2%, respectively. The endothermic and spontaneous adsorption was observed to trail the pseudo-second-order kinetics under optimized process parameters. Thus, the chemically modified walnut shell powder can be an eco-friendly adsorbent for Cr(VI) from aqueous solutions.
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Juglans , Poluentes Químicos da Água , Águas Residuárias , Adsorção , Pós , Cromo/análise , Água , Cinética , Concentração de Íons de Hidrogênio , Poluentes Químicos da Água/análise , TermodinâmicaRESUMO
Biochar can be used for soil remediation in environmentally beneficial manner, especially when combined with nanomaterials. After a decade of research, still, no comprehensive review was conducted on the effectiveness of biochar-based nanocomposites in controlling heavy metal immobilization at soil interfaces. In this paper, the recent progress in immobilizing heavy metals using biochar-based nanocomposite materials were reviewed and compared their efficacy against that of biochar alone. In details, an overview of results on the immobilization of Pb, Cd, Cu, Zn, Cr, and As was presented by different nanocomposites made by various biochars derived from kenaf bar, green tea, residual bark, cornstalk, wheat straw, sawdust, palm fiber, and bagasse. Biochar nanocomposite was found to be most effective when combined with metallic nanoparticles (Fe3O4 and FeS) and carbonaceous nanomaterials (graphene oxide and chitosan). This study also devoted special consideration to different remediation mechanisms by which the nanomaterials affect the effectiveness of the immobilization process. The effects of nanocomposites on soil characteristics related to pollution migration, phytotoxicity, and soil microbial composition were assessed. A future perspective on nanocomposites' use in contaminated soils was presented.
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Metais Pesados , Nanoestruturas , Poluentes do Solo , Poluentes do Solo/análise , Metais Pesados/análise , Carvão Vegetal , Solo , CádmioRESUMO
Excessive phosphorus causes eutrophication problems. The adsorptive removal of phosphate is prevalent and practical in large-scale applications, such as column adsorption. A metal organic framework (MOF)-enhanced layered double hydroxide (LDH) adsorbent material was developed and studied for batch adsorption and then combined with polyacrylonitrile (PAN) to form MOF/LDH/PAN composite beads working as a functional material for columns. Scanning electron microscopy (SEM) images showed the well-dispersed adsorbent powder in porous composite beads. The Fowler-Guggenheim isotherm model described the phosphate adsorption behavior of the MOF/LDH powder with a maximum capacity of 74.96 mg P/g. Mass transfer in the composite beads was successfully described with the Fickian diffusion model. The composite-packed fixed bed treated 37.95 BVs of the influent (55.51 mg P/L phosphate solution) and achieved an uptake of 18.92 mg P/g, with a removal efficiency of 96.42%, before the breakthrough point in the column study. The phosphate-loaded composite bed was regenerated with 0.1 M NaOH to 70% efficiency within 30 BVs. The polymer composite can be considered a practical solution for adsorption-based water treatment applications in tank and column processes where powder adsorbents cannot be applied.
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Estruturas Metalorgânicas , Poluentes Químicos da Água , Fosfatos , Pós , Poluentes Químicos da Água/análise , Hidróxidos , Adsorção , CinéticaRESUMO
The excess sludge from municipal sewage treatment plants is rich in Fe (III) due to chemical dephosphorization. The activation of peroxymonosulfate (PMS) by biochar derived from anaerobic and aerobic iron-containing excess sludge was studied systematically in this research. Fe (III)-containing excess sludge was cultured in an anaerobic environment for conversion of partial Fe (III) to Fe (II), which was further carbonized to prepare biochar labeled AnSx@Fe. Meanwhile, aerobic sludge with different Fe (III) content was directly carbonized to produce biochar labeled AeS@Fe. For biochar (AnS20@Fe-15%) prepared from 15% Fe(III)-containing anaerobic cultured 20 days sludge, the relative contents of Fe (III) and Fe (II) were 21.26% and 78.74%, which were 31.03% and 68.97% for biochar (AeS@Fe-10%) prepared from 10% Fe (III)-containing aerobic sludge. Fe (III) can be reduced to Fe (II) by both anaerobic culture and carbonization. Their removal rates of tetracycline (TC) through 60 min PMS activation were 97% and 98%, with TOC (Total organic carbon) removal of 61.8% and 53.4% respectively. The reactive species including sulfate radical [Formula: see text], hydroxyl radical (·OH) and singlet oxygen (1O2) were produced during PMS activation. After O2-aeration treatment of both AeS@Fe and AnSx@Fe, the relative content of Fe (II) was decreased and group C = O was disappeared, which resulted in reduction of [Formula: see text], ·OH and 1O2. The generation of [Formula: see text] and ·OH was dominated by the Fe (II) activation and the 1O2 generation was originated from graphite type N and C = O. Direct carbonization of aerobic and anaerobic sludge is a feasible method to produce biochar for PMS activation.
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Ferro , Esgotos , Ferro/química , Anaerobiose , Peróxidos/química , Carvão VegetalRESUMO
Hydrogen production using polymer membrane electrolyzers is an effective and valuable way of generating an environmentally friendly energy source. Hydrogen and oxygen generated by electrolyzers can power drone fuel cells. The thermodynamic analysis of polymer membrane electrolyzers to identify key losses and optimize their performance is fundamental and necessary. In this article, the process of the electrolysis of water by a polymer membrane electrolyzer in combination with a concentrated solar system in order to generate power and hydrogen was studied, and the effect of radiation intensity, current density, and other functional variables on the hydrogen production was investigated. It was shown that with an increasing current density, the voltage generation of the electrolyzer increased, and the energy efficiency and exergy of the electrolyzer decreased. Additionally, as the temperature rose, the pressure dropped, the thickness of the Nafion membrane increased, the voltage decreased, and the electrolyzer performed better. By increasing the intensity of the incoming radiation from 125 W/m2 to 320 W/m2, the hydrogen production increased by 111%, and the energy efficiency and exergy of the electrolyzer both decreased by 14% due to the higher ratio of input electric current to output hydrogen. Finally, machine-learning-based predictions were conducted to forecast the energy efficiency, exergy efficiency, voltage, and hydrogen production rate in different scenarios. The results proved to be very accurate compared to the analytical results. Hyperparameter tuning was utilized to adjust the model parameters, and the models' results showed an MAE lower than 1.98% and an R2 higher than 0.98.
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In the current study, cellulose/MoS2/GO nanocomposite has been synthesized by a hydrothermal method. Reports published regarding efficiency of Mo and graphene oxide-based nanocomposites for environmental remediation motivated to synthesize cellulose supported MoS2/GO nanocomposite. Formation of nanocomposite was initially confirmed by UV-visible and FTIR spectroscopic techniques. Particle size and morphology of the nanocomposite were assessed by scanning electron microscopy (SEM), and it was found having particle size ranging from 50 to 80 nm and heterogeneous structure. The XRD analysis also confirmed the structure of the nanocomposite having cellulose, MoS2, and GO. The synthesized nanocomposite was further tested for biomolecule protective potential employing different radical scavenging assays. Results of radical DPPHâ (50%) and ABTS â+ (51%) scavenging studies indicate that nanocomposites can be used as a biomolecule protective agent. In addition, nanocomposite was also evaluated for photocatalytic potential, and the results showed excellent photocatalytic properties for the degradation of 4-nitrophenol up to 75% and methylene blue and methyl orange up to 85% and 70%, respectively. So, this study confirmed that cellulose supported/stabilized MoS2/GO nanocomposite can be synthesized by an ecofriendly, cost-effective, and easy hydrothermal method having promising biomolecule protective and photocatalytic potential.
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In the present research work, selective and sensitive catechol (CT) detection and quantification were shown in the presence of resorcinol (RS) in 0.2 M phosphate buffer (PB) solution by preparing a low-cost, simple, and green carbon nanotube paste electrode (CNTPE) surface activated with electropolymerized riboflavin (PRF). The morphological, conductivity, and electrochemical features of the modified electrode (PRFMCNTPE) and bare carbon nanotube paste electrode (BCNTPE) materials were analyzed using electrochemical impedance spectroscopy (EIS), field emission scanning electron microscopy (FE-SEM), cyclic voltammetry (CV), and differential pulse voltammetry (DPV). The PRF-activated electrode displays outstanding sensitivity, stability, selectivity, reproducibility, and repeatability for the redox feature of CT with improved electrochemical current and declined electrochemical potential compared to BCNTPE. The peak currents of CT are correlated to the different CT concentrations (CV method: 6.0-60.0 µM & DPV method: 0.5-7.0 µM), and the obtained detection limit (DL) and quantification limit (QL) are found to be 0.025 µM and 0.085 µM (CV method) and 0.0039 µM and 0.0132 µM (DPV method), respectively. The prepared PRFMCNTPE material was advantageous for the examination of CT in environmentally important tap water sample as a real-time application.
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This work successfully utilised eco-friendly green synthesis to produce Ag-TiO2 nanofibers (NFs). As pollution and energy limitations have become global issues, there is an ongoing need to develop more effective catalysts through straightforward and environmentally friendly methods. The Ag-TiO2 nanofibers (NFs) XRD pattern exhibits an anatase TiO2 and FCC crystal structure of Ag nanoparticles. The SEM investigation revealed a nanofiber-like surface morphology. The Ag-TiO2 nanofibers (NFs) exhibits an optical band gap energy is 2.5 eV. Methylene blue (MB), malachite green (MG), Congo red (CR), and crystal violet (CV) dye aqueous solutions were used to evaluate the photocatalytic performance of the synthesized Ag-modified TiO2 nanofibers (NFs) under direct sunlight irradiation. The effects of catalyst size on the efficient breakdown of MB dye were also investigated. The optimum catalyst concentration was found to be at 0.02 mg/mL. At 120 min of direct sunlight, the highest photosynthetic degradation efficiency (DE percentage) of 94% was achieved for MB dye. Ag-TiO2 nanofibers (NFs) have been demonstrated to have exceptional antibacterial activity against Gram-positive bacteria such as Staphylococcus aureus and Gram-negative bacteria E-Coli. Because of these great qualities, it seems likely that the Ag-TiO2 nanofibers (NFs) made could be a great photocatalyst for getting dye pollutants out of wastewater.
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Nanopartículas Metálicas , Nanofibras , Nanofibras/química , Nanopartículas Metálicas/química , Prata/química , Titânio/química , Antibacterianos/químicaRESUMO
This work prepared a composite of orange peels magnetic activated carbon (MG-OPAC). The prepared composite was categorized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), Brunauer-Emmett-Teller (BET), Energy-dispersive X-ray spectroscopy (EDX), Scanning Electron Microscopy (SEM) and vibrating-sample magnetometer (VSM) analyses. The MG-OPAC composite showed the surface area (155.09 m2/g), the total volume of pores (0.1768 cm3/g), and the mean diameter of pores (4.5604 nm). The saturation magnetization (Ms = 17.283 emu/g), remanence (Mr = 0.28999 emu/g) and coercivity (Hc = 13.714 G) were reported for the prepared MG-OPAC. Likewise, at room temperature, the MG-OPAC was in a super-paramagnetic state, which could be collected within 5 S (< 5 S) with an outside magnetic field. Influence of time of contact, absorbent dose, starting concentration of Cr6+ ions, and pH were tested to adjust the absorption process. The absorption behavior of MG-OPAC for hexavalent chromium was investigated by Langmuir (LIM), Freundlich (FIM) and Temkin (TIM) isotherm models (IMs). Applicability of LIM specifies that Cr6+ ions absorption procedure may be monolayer absorption. The maximum monolayer capacity (Qm) premeditated by LIM was 277.8 mg/g. Similarly, the absorption process was tested with different kinetic models like intraparticle diffusion (IPDM), pseudo-first-order (PFOM), Elovich (EM), pseudo-second-order (PSOM), and Film diffusion (FDM). The PSOM was best fitted to the experimental results of Cr6+ ions absorption with R2 ranging between 0.992 and 1.
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Urbanization and a massive population boom have immensely increased the solid wastes (SWs) generation and are expected to reach 3.40 billion tons by 2050. In many developed and emerging nations, SWs are prevalent in both major and small cities. As a result, in the current context, the reusability of SWs through various applications has taken on added importance. Carbon-based quantum dots (Cb-QDs) and their many variants are synthesized from SWs in a straightforward and practical method. Cb-QDs are a new type of semiconductor that has attracted the interest of researchers due to their wide range of applications, which include everything from energy storage, chemical sensing, to drug delivery. This review is primarily focused on the conversion of SWs into useful materials, which is an essential aspect of waste management for pollution reduction. In this context, the goal of the current review is to investigate the sustainable synthesis routes of carbon quantum dots (CQDs), graphene quantum dots (GQDs), and graphene oxide quantum dots (GOQDs) from various types SWs. The applications of CQDs, GQDs, and GOQDs in the different areas are also been discussed. Finally, the challenges in implementing the existing synthesis methods and future research directions are highlighted.
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Grafite , Pontos Quânticos , Carbono , Resíduos SólidosRESUMO
Spar caps, which cover 50% of the cost of windmill blades, were made of unidirectional and biaxial glass/carbon reinforcements of 600 gsm with thicknesses ranging from 100 to 150 mm for blades 70-80 m long. The significance of this study was to utilize an economical biodegradable material i.e bamboo fabric of 125 gsm to fabricate a lightweight composite and study its behavior for spar caps applications. The aim of this research was to investigate the effect of weave pattern and composite size at coupon level under thermal, dynamic, water absorption, and flammability conditions. Composites comprising 125 gsm plain and twill weave bamboo as reinforcements/AI 1041 Phenalkamine bio-based hardener with epoxy B-11 as matrix were tested. Thermo-Gravimetric Analysis revealed that the weave pattern and composite thickness had an effect on the rate of weight loss and sustenance until 450 °C. The pattern had an effect on the glass transition temperature, as seen by Differential Scanning Calorimetry. The weave pattern and size thickness had an effect on energy storage and dissipation, displaying the damping behavior in DMA. The weave pattern and size had an effect on the rate of water absorption, which saturated after a few hours. The wettability and thickness of composites hampered the burning rate, with 5.4 mm thickness resulting in a 30% decrease.
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Adsorption is the most widely used technique for advanced wastewater treatment. The preparation and application of natural renewable and environmentally friendly materials makes this process easier and more profitable. Chitosan is often used as an effective biomaterial in the adsorption world because of its numerous functional applications. Chitosan is one of the most suitable and functionally flexible adsorbents because it contains hydroxyl (-OH) and amine (-NH2) groups. The adsorption capacity and selectivity of chitosan can be further improved by introducing additional functions into its basic structure. Owing to its unique surface properties and adsorption ability of chitosan, the development and application of chitosan nanomaterials has gained significant attention. Here, recent research on chitosan nanoparticles is critically reviewed by comparing various methods for their synthesis with particular emphasis on the role of experimental conditions, limitations, and applications in water and wastewater treatment. The recovery of pollutants using magnetic nanoparticles is an important treatment process that has contributed to additional development and sustainable growth. The application of such nanoparticles in the recovery metals, which demonstrates a "close loop technology" in the current scenarios, is also presented in this review.
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BACKGROUND: Food hygiene is one of the specialized fields of environmental health, and despite the problems associated with foodborne illnesses, there is no evaluation available that would focus on specialized environmental health journals. The purpose of the present survey is a comparison of the status of food hygiene articles published in Iranian and international journals of environmental health. METHODS: This cross-sectional descriptive study was performed on all published articles in five Iranian environmental health journals and three international environmental health journals that are among the top 5% and 10% based on SNIP, emphasizing the issue of food. Our data were collected by searching relevant keywords in the articles published during the years (2008-2021), with emphasis on food hygiene. In the checklist, journal and articles information was collected by year of publication, a number of articles, information on authors' participation status in terms of number, gender, organizational affiliation, country and continents, and research centers according to authors' authorship. Statistical analysis of data was performed using descriptive and inferential statistical indices. VOSviewer software was also used to visualize the data. RESULTS: In Iranian environmental health journals, out of 2305 articles (7.3%) and out of 6898 articles in international environmental health journals (2.4%) dealt with food hygiene. Food hygiene articles were divided into seven categories, with the largest number of articles on aquatic and agricultural products each with a frequency of 48 articles. Articles related to heavy metals in food were provided by 30.81%. In this study, out of 150 articles, 15 articles were written with the participation of 30 authors from seven continents (Asia, America, and Europe), most of which were from Asia and India. In international environmental health journals, among the main research topics in articles related to food hygiene, the highest number (52.5%) was related to a determination about pollution such as heavy metal concentrations in food. CONCLUSIONS: Articles published in Iranian and international environmental health journals about food hygiene were limited. According to the increasing prevalence of foodborne illnesses, especially in recent decades, and the importance of paying attention to food hygiene, more targeted studies are needed.
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Publicações Periódicas como Assunto , Humanos , Irã (Geográfico) , Estudos Transversais , Bibliometria , ÁsiaRESUMO
The introduction of unintended oil spills into the marine ecosystem has a significant impact on aquatic life and raises important environmental concerns. The present review summarizes the recent studies where nanocomposites are applied to treat oil spills. The review deals with the techniques used to fabricate nanocomposites and identify the characteristics of nanocomposites beneficial for efficient recovery and treatment of oil spills. It classifies the nanocomposites into four categories, namely bio-based materials, polymeric materials, inorganic-inorganic nanocomposites, and carbon-based nanocomposites, and provides an insight into understanding the interactions of these nanocomposites with different types of oils. Among nanocomposites, bio-based nanocomposites are the most cost-effective and environmentally friendly. The grafting or modification of magnetic nanoparticles with polymers or other organic materials is preferred to avoid oxidation in wet conditions. The method of synthesizing magnetic nanocomposites and functionalization polymer is essential as it influences saturation magnetization. Notably, the inorganic polymer-based nanocomposite is very less developed and studied for oil spill treatment. Also, the review covers some practical considerations for treating oil spills with nanocomposites. Finally, some aspects of future developments are discussed. The terms "Environmentally friendly," "cost-effective," and "low cost" are often used, but most of the studies lack a critical analysis of the cost and environmental damage caused by chemical alteration techniques. However, the oil and gas industry will considerably benefit from the stimulation of ideas and scientific discoveries in this field.
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Nanocompostos , Poluição por Petróleo , Poluição por Petróleo/análise , Ecossistema , Óleos , PolímerosRESUMO
Photocatalysis is considered a useful technique employed for the dye degradation through solar light, visible or UV light irradiation. In this study, TiO2, g-C3N4, and TiO2-g-C3N4 nanocomposites were successfully synthesized and studied for their ability to degrade Rhodamine B (RhB) and Reactive Orange 16 (RO-16), when exposed to visible light. The analytical techniques including XRD, TEM, SEM, DRS, BET, XPS, and fluorescence spectroscopy were used to explore the characteristics of all the prepared semiconductors. The photocatalytic performance of synthesized materials has been tested against both the selected dyes, and various experimental parameters were studied. The experimental results demonstrate that, in comparison to other fabricated composites, the TiO2-g-C3N4 composite with the optimal weight ratio of g-C3N4 (15 wt%) to TiO2 has shown outstanding degrading efficiency against RhB (89.62%) and RO-16 (97.20%). The degradation experiments were carried out at optimal conditions such as a catalyst load of 0.07 g, a dye concentration of 50 ppm, and a temperature of 50 â at neutral pH in 90 min. In comparison to pure TiO2 and g-C3N4, the TiO2-g-C3N4, a semiconductor, has shown higher degradation efficiency due to its large surface area and decreased electron-hole recombination. The scavenger study gave an idea about the primary active species (-OH radicals), responsible for dye degradation. The reusability of TiO2-g-C3N4 was also examined in order to assess the composite sustainability.
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Corantes , Luz , Raios Ultravioleta , Titânio/químicaRESUMO
The COVID-19 outbreak led to the discovery of SARS-CoV-2 in sewage; thus, wastewater treatment plants (WWTPs) could have the virus in their effluent. However, whether SARS-CoV-2 is eradicated by sewage treatment is virtually unknown. Specifically, the objectives of this study include (i) determining whether a mixed matrixed membrane (MMM) is able to remove SARS-CoV-2 (polycarbonate (PC)-hydrous manganese oxide (HMO) and PC-silver nanoparticles (Ag-NP)), (ii) comparing filtration performance among different secondary treatment processes, and (iii) evaluating whether artificial neural networks (ANNs) can be employed as performance indicators to reduce SARS-CoV-2 in the treatment of sewage. At Shariati Hospital in Mashhad, Iran, secondary treatment effluent during the outbreak of COVID-19 was collected from a WWTP. There were two PC-Ag-NP and PC-HMO processes at the WWTP targeted. RT-qPCR was employed to detect the presence of SARS-CoV-2 in sewage fractions. For the purposes of determining SARS-CoV-2 prevalence rates in the treated effluent, 10 L of effluent specimens were collected in middle-risk and low-risk treatment MMMs. For PC-HMO, the log reduction value (LRV) for SARS-CoV-2 was 1.3-1 log10 for moderate risk and 0.96-1 log10 for low risk, whereas for PC-Ag-NP, the LRV was 0.99-1.3 log10 for moderate risk and 0.94-0.98 log10 for low risk. MMMs demonstrated the most robust absorption performance during the sampling period, with the least significant LRV recorded in PC-Ag-NP and PC-HMO at 0.94 log10 and 0.96 log10, respectively.