Hazardous Pollutants Research Articles

Development of simplistic and stable Co-doped ZnS nanocomposite towards excellent removal of bisphenol A from wastewater and hydrogen production: Evaluation of reaction parameters by response surface methodology

BackgroundEnvironmentally friendly and sustainable approaches for the removal of hazardous pollutants from wastewater continue to be explored. The present study presents the novel Co-ZnS nanocomposites which were synthesized by the ethanolic crude extract of Oxystelma esculentum and then successfully evaluated towards degradation of Bisphenol A and hydrogen production. The synthesized nanocomposites were systematically characterized by multiple state-of-the-art experimental techniques. MethodsThe present study illustrates the green synthesis of Co-doped ZnS nanocomposites and their promising potential for photodegradation of BPA and hydrogen production. The nanocomposite shows an excellent potential for BPA degradation (0.052 min−1) and hydrogen evolution (3157.9 µmolh−1 g−1). The detailed optimized analysis of synthesized nanocomposite demonstrates remarkable abilities to degrade organic pollutants by applying a “response surface methodology” model. Significant FindingsThe optimized value of the photocatalyst along with optimized parameters presented considerable photocatalytic activity for the degradation of BPA (94.69 %) and the value of hydrogen (3157.9 µmolh−1 g−1). Then, the confirmation of the results (theoretical and experimental yield) was carried out by RSM. The RSM indicated the predicted D % value of 96.84 % via the developed model with the optimized conditions of pH = 5.146, BPA dose = [53.448 mg/L], Photocatalyst dose = [58.3058 mg], and temperature = 32.2673 °C. The pHzpc of the prepared photocomposites was found to be ∼6.9.

Green biosynthesized N-doped CuO@Zeolite nanocomposite for the efficient photodegradation of toxic organic pollutants from wastewater

Nanotechnology is one of the most advanced methods available for the degradation of toxic pollutants from the environment. Specifically, nanoparticles generated with plant extracts are more stable and biocompatible than those produced using traditional chemical and physical processes. The current study focuses on the green synthesis of N-CuO@Zeolite nanocomposite with Camellia sinensis (green tea) leaf extract. The green synthesized nanocomposite was used for the photocatalytic degradation of hazardous organic pollutants, including Auramine-O (AO) and yellow color textile industrial dye (YD). Under direct sunlight irradiation, synthesized nanomaterials exhibited excellent photocatalytic activity for AO and YD degradation. The best conditions for photocatalytic degradation were found to be pollutant concentrations of 2 mg L−1 for AO and 6 mg L−1 for YD, photocatalyst dosages of 15 mg for both AO and YD, and neutral pH for both pollutants. Within 150 minutes, the synthesized N-CuO@zeolite nanocomposite attained degradation efficiencies of 95 % for AO and 92 % for YD, compared to its parent materials N-CuO (80 % for AO and 76 % for YD) and CuO (68 % for AO and 65 % for YD). The degradation rates of both pollutants were accurately described by first-order kinetics, consistent with the Langmuir adsorption model. Additionally, the ecologically sustainable novel N-CuO@Zeolite nanocomposite illustrated superior reliability and reusability, keeping photocatalytic efficiency even after ten cycles of constant utilization, and its long-term stability was confirmed by PXRD analysis after processing. The material's excellent reusability and stability emphasize the nanocomposite's potential as a long-term solution for industrial wastewater treatment applications.

Porphyrin-Grafted Poly(ethylene terephthalate) as a Reusable and Highly Selective Colorimetric Probe for Mercuric Ion Contaminants in Aqueous Samples.

Heavy metals are the most hazardous water pollutants, with severe health and environmental consequences. Among these, mercuric (Hg2+) ions are known to cause detrimental health issues in both humans and aquatic life. Due to this, several analytical techniques have been devised to detect and quantify the amount of this ion. However, most of these require advanced instrumentation, prolonged analysis time, and sample preparation. In this study, a low-cost and highly reusable colorimetric probe was developed by grafting porphyrin to poly(ethylene terephthalate) sheets using an oxazoline polymer as covalent adhesive. Upon exposure to trace amounts of Hg2+ in solution, the fabricated material visually transitioned from faint brownish pink to green by the complexation mechanism. Additionally, the transparency of this probe allowed the quantitative spectrophotometric determination of the Hg2+ concentration in aqueous samples. It was also shown that the material is highly stable, which can be reused for more than 50 times without significant decline in its performance, hence, making it suitable for the onsite monitoring of mercuric ion contamination in different bodies of water.

Influence of Western Pacific Madden–Julian Oscillation on New York City's Record‐Breaking Air Pollution in Early June 2023

AbstractIn early June 2023, New York City (NYC) and other cities in the northeastern US experienced a severe air pollution event. Although reports associated this hazardous pollution event with the smoke from Canadian wildfires, the factors triggering the southward waft of the smoke remain unclear. We found the northerly anomaly that transported the smoke was linked to the Rossby wave train excited by the Madden–Julian Oscillation (MJO) over the Philippine Sea, which led to the formation of an enhanced northerly at the western edge of the cyclonic anomaly over the East Coast–North Atlantic. When the MJO convection left the western Pacific, the disorganized teleconnection caused the pollution to dissipate. Observational findings were further supported by model simulations and predictions. These results suggest that monitoring and predictions of MJO activity may help mitigate air pollution events over the northeastern US during Canadian wildfire seasons.

A fascinating exploration into nitrite accumulation into low concentration reactors using cutting-edge machine learning techniques

In the last couple decades, more use of nitrogenous chemical fertilizers and improper disposable of wastewater has harmed water and it cause water pollution. Low concentrated Nitrite (NO2) is the one of hazardous pollution and it is difficult to remove through biological processes, while it occurs in low concentration. Many technologies have been developed to accumulate NO2 in the mainstream. However, most of them use chemical inhibitors for nitrite oxidizing bacteria (NOB). In past studies high concentrated reactor performance have been modeled using mathematical models. In this study, machine learning application (MLA) was applied to model the performance of reactors. The reactor was low concentrated, continuous stirred tank reactor (CSTR) with in-fluent total ammonia nitrogen (TAN) concentration was (∼30PPM-TAN and ∼50PPM-TAN) and lower output TAN concentration was (∼1PPM-TAN). However, 216 days of water treatment data from CSTR were used, and the CSTR’s efficiency (%) of nitrite accumulation was estimated using in-fluent and effluent quantities. Then efficiency is predicted with 70 % of the data that is used to train the algorithms. Confusion matrix was used to access the performance of algorithms and actual and predicted classes (efficiencies) were compared. The DTC and XGB over-performed other algorithms.

Tungsten phosphide: a high-performance catalyst for determination of p-nitrophenol, a hazardous water pollutant

Tungsten phosphide: a high-performance catalyst for determination of p-nitrophenol, a hazardous water pollutant

A novel indicator for lead poisoning beyond blood lead level: Facile diagnosis of lead poisoning using random urine with point-of-care testing

Lead (Pb) poisoning is estimated to account for 1 % of the global disease burden. The gold standard for diagnosing lead poisoning in human body relies on blood lead level (BLL), which is always performed in hospitals using expensive instruments. However, there are still many countries and regions with a lack of medical resources (without enough professional medical staff and analytical instruments). To achieve a facile diagnosis of lead poisoning by ordinary residents (without any expertise), this study conducted a research study on 810 participants to discover and validate a new lead poisoning indicator (creatinine-corrected urinary lead level, cULL) beyond BLL in non-invasive samples. A point-of-care testing (POCT) device to measure cULL was developed, equipped with liquid-phase microextraction and electromembrane extraction on a paper-based analytical device for on-site separation of lead and creatinine in the urine, using a smartphone for the quantification of analytes. The cULL as a novel indicator and the POCT device developed could be effective in reducing the risk of damage from lead contamination.

Hazardous wildfire smoke events can alter dawn soundscapes in dry forests of central and eastern Washington, United States

As global wildfire activity increases, wildlife are facing greater exposure to hazardous smoke pollution – with unknown consequences for biodiversity. Research on the effects of smoke on wild animals is extremely limited, in part due to the inherent logistical challenges of observing how animals respond to smoke in real time. Passive acoustic monitoring may be a powerful tool to safely and effectively monitor biodiversity before, during, and after major smoke events. In this study, we used data collected from a large-scale network of bioacoustic recorders at 92 sites in central and eastern Washington state during August–September, 2019–2020 to investigate the effect of wildfire smoke on dawn soundscapes and, by extension, acoustically active wildlife. We used acoustic indices to document and characterize changes in soundscapes related to smoke exposure, including the Acoustic Complexity Index (ACI), Bioacoustic Index (BI), and Normalized Difference Soundscape Index (NDSI). Higher values of these indices likely indicate higher levels of biodiversity in our study area. We hypothesized that wildfire smoke would reduce bird vocalizations, leading to declines in ACI, BI, and NDSI at dawn, when birds are most active. We used linear and quantile regression models to test for an effect of daily exposure to fine particulate matter (PM2.5), a marker of wildfire smoke, on the mean daily values and the upper 90th percentile of each index at dawn. We also conducted a before-during-after analysis of a particularly hazardous smoke event that impacted our study area on September 12–14, 2020. We did not observe linear effects of daily PM2.5 on average or peak daily values of acoustic indices; however, we did observe a significant reduction in ACI and BI during the three-day smoke event in 2020 and in the two weeks following this air pollution episode. Our results indicate that, on average, ACI and BI were reduced by 2.7 % and 15.9 % during and 1.5 % and 11.0 % afterward, respectively. These findings add further evidence that wildfire smoke alters soundscapes, likely due to changes in the presence, abundance, or behavior of acoustically active animals. Furthermore, our study demonstrates that wildfire smoke may have delayed and/or cumulative effects on acoustically active wildlife. Our study highlights the potential for passive acoustic monitoring to document wildlife responses to smoke pollution and identify potentially relevant exposure periods.

Chalcogen Bonding in Selective Recognition and Liquid-Liquid Extraction of Perrhenate.

Efficient recognition and extraction of hazardous anionic pollutants from water medium is of great significance for environmental concerns, representing a challenging area of research in supramolecular chemistry. In this study, we present, for the first time, a comprehensive demonstration of the ability of chalcogen bonding (ChB) to recognize and remove the ReO4 - from 100 % water medium. The anion recognition ability is well elucidated through solution phase NMR and ITC studies, which clearly reveal the selective binding of ReO4 - over other oxo-anions. Moreover, the selenoimidazolium scaffold effectively engages in Se•••O ChB interaction with ReO4 - as confirmed by X-ray crystal structure and XPS analysis. More importantly, the binding of ReO4 - with different prolongations of the σ-holes, along with Se•••Se chalcogen bonding interactions, lead to the formation of a 1D supramolecular assembly. Eventually, ChB receptor Se4Me-Br exhibits ~62 % ReO4 - extraction efficiency through precipitation as the extraction method. Furthermore, in efforts to enhance efficiency, a hydrophobic ChB receptor Se4Do-PF6 has been prepared, achieving an efficiency of up to ~93 % at a very low concentration (~5 ppm) by liquid-liquid extraction.

Molecular insights into the catalytic mechanism of a phthalate ester hydrolase

Phthalate esters (PAEs) are emerging hazardous and toxic chemicals that are extensively used as plasticizers or additives. Diethyl phthalate (DEP) and dimethyl phthalate (DMP), two kinds of PAEs, have been listed as the priority pollutants by many countries. PAE hydrolases are the most effective enzymes in PAE degradation, among which family IV esterases are predominate. However, only a few PAE hydrolases have been characterized, and as far as we know, no crystal structure of any PAE hydrolases of the family IV esterases is available to date. HylD1 is a PAE hydrolase of the family IV esterases, which can degrade DMP and DEP. Here, the recombinant HylD1 was characterized. HylD1 maintained a dimer in solution, and functioned under a relatively wide pH range. The crystal structures of HylD1 and its complex with monoethyl phthalate were solved. Residues involved in substrate binding were identified. The catalytic mechanism of HylD1 mediated by the catalytic triad Ser140-Asp231-His261 was further proposed. The hylD1 gene is widely distributed in different environments, suggesting its important role in PAEs degradation. This study provides a better understanding of PAEs hydrolysis, and lays out favorable bases for the rational design of highly-efficient PAEs degradation enzymes for industrial applications in future.

Boosted photocatalytic performance of cobalt ferrite anchored g-C3N4 nanocomposite toward various emerging environmental hazardous pollutants degradation: insights into stability and Z-scheme mechanism.

In this study, a highly efficient CoFe2O4-anchored g-C3N4 nanocomposite with Z-scheme photocatalyst was developed by facile calcination and hydrothermal technique. To evaluate the crystalline structure, sample surface morphology, elemental compositions, and charge conductivity of the as-synthesized catalysts by various characterization techniques. The high interfacial contact of CoFe2O4 nanoparticles (NPs) with g-C3N4 nanosheets reduced the optical bandgap from 2.67 to 2.5eV, which improved the charge carrier separation and transfer. The photo-degradation of methylene blue (MB) and rhodamine B (Rh B) aqueous pollutant suspension under visible-light influence was used to investigate the photocatalytic degradation activity of the efficient CoFe2O4/g-C3N4 composite catalyst. The heterostructured spinel CoFe2O4 anchored g-C3N4 photocatalysts (PCs) with Z-scheme show better photocatalytic degradation performance for both organic dyes. Meanwhile, the efficiency of aqueous MB and Rh B degradation in 120 and 100min under visible-light could be up to 91.1% and 73.7%, which is greater than pristine g-C3N4 and CoFe2O4 catalysts. The recycling stability test showed no significant changes in the photo-degradation activity after four repeated cycles. Thus, this work provides an efficient tactic for the construction of highly efficient magnetic PCs for the removal of hazardous pollutants in the aquatic environment.

Characterization of a Bacterial Keratinolytic Protease for Effective Degradation of Chicken Feather Waste into Feather Protein Hydrolysates.

Chicken feathers contribute to large quantities of keratinaceous wastes that pose serious environmental problems and must be catered to properly. Chicken feathers are also a potential source of vital proteins, peptides, and amino acids, which could be used as low-cost animal feeds. Therefore, there has been increasing interest in keratinase-producing microbes for reprocessing and using keratinous biomaterials. Among the five isolated keratinolytic microorganisms, one microbe, Bacillus XT 01, produced a significant amount of enzyme activity, which was partially characterized. The potential of this protease-producing microbe was investigated for converting feather keratin waste to valuable protein hydrolysate. Maximum keratinase production was observed after 5 days of incubating Bacillus XT 01 at an optimum temperature of 45 °C and pH 8.5. Sodium Dodecyl Sulphate-Polyacrylamide Gel Electrophoresis (SDS-PAGE) and zymogram of ammonium sulfate precipitated culture supernatant showed the presence of several proteolytic enzymes with molecular weights between 30 and 60 kDa. The Bacillus strain caused almost complete feather degradation (98%) after 7 days of incubation at 45 °C in a shake culture medium. Antioxidant and reducing activities of the feather protein hydrolysate (FPH) elevated with increased cultivation time. Investigation of the effect of feather protein hydrolysate on plants indicated improved plant growth regarding the agronomic parameters, such as plant height, number of trifoliate leaves, number of pods, pod length, number of seeds per pod, and root length, which increased by 30.84%, 49.32%, 70.90%, 53.27%, 60.03%, and 54.71%, respectively. The prospective of Bacillus XT 01 for degrading feather waste keratin to highly valued hydrolyzed feather protein offers effectiveness in the poultry industry and ultimately decreases environmental pollution hazards.

Biochar produced from waste‐based feedstocks: Mechanisms, affecting factors, economy, utilization, challenges, and prospects

AbstractBiochar possesses unique characteristics, including a substantial surface area, a high carbon content, sufficient capacity for cation exchange, and a robust structure. However, biochar contains hazardous pollutants like volatile organic compounds that harm soil properties and functionality. Although several studies on biochar production from various feedstocks have been undertaken in recent years, several issues about feedstock preparation, economic feasibility, influencing factors, and the proper utilization of biochar production processes need to be addressed. This paper thus addresses these issues by providing potential solutions identified through a comprehensive review. Slow pyrolysis of lignocellulosic biomass and Acacia nilotica yields biochar from 20 to 52 wt% at various temperatures and residence times. Biochar yield varies from 29 to 48.3 wt% when waste tires and corn stalks are rapidly pyrolyzed at higher temperatures and for shorter periods. Torrefaction of algal biomass at moderate temperatures with different residence times can result in a substantial yield of 50–60 wt%. However, the variability and heterogeneity of waste feedstocks pose potential challenges affecting biochar's quality and properties. Given its widespread use in carbon sequestration, soil remediation, wastewater purification, and organic waste composting, the mechanisms of biochar production in environmental usage need to be investigated.

Construction of coal fly ash-based spherical grain adsorbents and their adsorption characteristics on phenolic compounds

Addressing the significant emissions and severe pollution hazards posed by coal fly ash waste in the coal chemical industry, as well as the challenges in recovering phenolic substances from coal chemical wastewater, this study utilized coal fly ash as a raw material to construct two types of spherical grain adsorbents: coal fly ash and coal gangue spherical grain (CFAGsg) and coal fly ash and pyrite spherical grain (CFAPsg). The adsorption performance of CFAGsg and CFAPsg towards phenolic substances in coal chemical wastewater was investigated. The research results demonstrated that CFAGsg and CFAPsg exhibited adsorption capacities of 20.31 mg/L and 30.42 mg/L for phenol, respectively, and maintained stable adsorption performance even after multiple regeneration cycles. Further analysis using kinetic, isotherm, and thermodynamic models, along with various characterization techniques, revealed that the adsorption of phenol onto CFAGsg and CFAPsg was primarily governed by physical and chemical adsorption, involving an endothermic reaction. Moreover, the study on the adsorption mechanism of phenol revealed that the adsorption behavior of CFAGsg and CFAPsg was mainly driven by pore filling, π-π stacking, and hydrogen bonding. Additionally, hydrophobic interactions were involved in the adsorption of phenol onto CFAGsg, while surface complexation forces played a role in the adsorption of phenol onto CFAPsg. Overall, the research findings provide vital theoretical support and practical application prospects for the high-value utilization of coal fly ash and the clean production of the coal chemical industry.

Green Technology Approach Towards the Removal of Heavy Metals, Dyes, and Phenols from Water Using Agro-based Adsorbents: A Review.

The swift pace of socioeconomic development and climatic change have put significant strain on the quality of water resources. While, the bulk availability of agro-based materials arising from nature and agricultural practices has paved the way for researchersin eradicating toxic industrial pollutants such as dyes, heavy-metals, phenolic-compounds, pesticides, etc. by using them as adsorbents. In the area of pollution remediation, inventive technologies have been developing. The adsorption technique stands out among the other wastewater-treatment methods as it is simple, easy, efficient, and cost-effective. The agro-based adsorbents their use in this area contributes to minimizing natural waste. They can be employed in their original raw-form or after undergoing simple processes such as drying, grinding, and carbonization. Moreover, these adsorbents are typically modified physically or chemically to change their surface properties and improve their adsorption efficiency. The low-cost agro adsorbents have shown efficient adsorption capacities towards removing various organic and hazardous water pollutants. With a few exceptions, majority of adsorbents have demonstrated heavy metals, dyes and phenol removal efficiencies exceeding 90%. This review summarizes the available information and strategies for using agro-based adsorbents to eliminate hazardous water pollutants. It is a prospective area for research in the field of environmental pollution.

Hydrothermally synthesized Nb -doped TiO2 nanosheets for efficient removal of methylene blue dye on photocatalytic performance

In this work, Niobium-doped (1%, 3%, and 5%) titanium dioxide (Nb-TiO2) nanosheets were successfully formed via the hydrothermal route and further characterized using TEM, XRD, XPS and UV–vis absorption spectroscopy techniques. Phase purity and structural information of the prepared materials were analysed by XRD measurements. The band gap values ranged from 3.27 to 2.98 eV as Nb doping increased, leading to improved photocatalytic activity by creating new energy levels close to the conduction band. The XPS results confirm the amalgamation of Nb5+ ions into TiO2 without affecting the crystallinity, structure or orientation of the occurrence of oxygen vacancies. In 3% Nb-doped TiO2, the degradation efficiency for removing (Methylene blue) MB dye increased by ∼96% for the removal of MB dye within 70 min in comparison to pure and other doped TiO2 catalysts The better photocatalytic activity of 3% Nb-TiO2 is due to the longer time between electron–hole pairs before they recombine into one pair. Hydroxyl radicals (HO•) and superoxide radicals (O2 •−) are the primary reactive entities responsible for the deterioration of MB dye. Therefore, incorporating Nb into TiO2 nanostructures represents an auspicious material for the decomposition of hazardous and toxic pollutants in aquatic environments.

Remarkable photodegradation breakdown cost, antimicrobial activity, photocatalytic efficiency, and recycling of SnO2 quantum dots throughout industrial hazardous pollutants treatment

In the conducted research, a one-step hydrothermal synthesis of pure and titanium-doped tin dioxide quantum dots is elaborated upon, with a thorough analysis of their structural, optical, morphological, and photocatalytic properties undertaken using advanced analytical techniques. Through X-ray Diffraction XRD, the crystalline nature and phase purity of the tetragonal structures of SnDs were confirmed, with the crystallite sizes measured at 3.0 nm for SnD1 and 7.66 nm for SnD2, following treatments at 240 °C and 300 °C, respectively. The structural integrity of SnO2 was maintained despite titanium doping. FTIR spectroscopy verified the existence of specific vibrational modes indicative of surface hydroxyl groups. HRTEM images revealed the spherical morphology of particles, with diameters of 3.5 nm for SnD1 and 9.1 nm for SnD2. Optical band gaps, determined through UV-DRS, ranged from 3.33 eV in SnD1 to 3.47 eV in SnDTi2. The photocatalytic degradation of Congo Red dye under xenon lamp irradiation was quantitatively assessed; notably, SnD1 exhibited a 23 % higher rate constant compared to SnD2, attributed to its smaller particle size and a 31 % greater surface area. Doping with 4 % Ti in Sn0.96Ti0.04O2 more than doubled the degradation rate compared to a 6 % Ti doping in Sn0.94Ti0.06O2. Furthermore, the generation of hydroxyl radicals was significantly enhanced, showing an increase of approximately 220 % for SnD1 and 80 % for SnD2. The capability of these nanomaterials to reduce the chemical oxygen demand of industrial organic pollutants to within regulatory limits under solar irradiation was documented, with SnD1 maintaining its photocatalytic efficiency over seven cycles of reuse. In the photocatalytic degradation rate of Congo Red dye, which was 23 % higher for SnD1 compared to SnD2, and the threefold increase in the degradation rate for SnDTi1 compared to SnDTi2. An economic assessment, based on electricity tariffs in Saudi Arabia, highlighted the cost-effectiveness of SnD1, which ranged from 26.93 to 30.36 USD per breakdown cost of the photodegradation process, showing it to be less costly than SnD2. Conversely, SnDTi1 was found to be more economical than SnDTi2, with costs ranging from 26.67 to 33.09 USD. Collectively, the results emphasize the outstanding photocatalytic performance and cost-efficiency of SnDs, reinforcing their potential as sustainable solutions for the treatment of industrial wastewater. Additionally, the antibacterial efficacy of these materials against a range of bacteria, yeast, and fungi was investigated and substantiated.

Harvesting surface (interfacial) energy for tribocatalytic degradation of hazardous dye pollutants using nanostructured materials: A review

AbstractIntroductionTribocatalysis, an emerging cutting‐edge technique that uses frictional mechanical energy to activate the catalytic operation of a reaction or material including nanomaterials has garnered the interest of the research community in recent times.AimThis study aimed to critically review original research works directed toward tribocatalytic degradation of various hazardous dye pollutants. Notably, in this review, various nanomaterials and their composites with outstanding tailored degradation profiles are explored for their tribocatalytic degradation efficiency for various dye pollutants. In addition, the effect of various operating factors that are of importance to engineers, industries, and investors for optimization purposes was pragmatically discussed. Also, the effect of electron trapping and radical scavengers alongside the mechanism of tribocatalytic degradation was empirically analyzed.ResultsFrom this work, it was found that the maximum tribocatalytic degradation efficiency was >80% in most cases at an optimum temperature of 20–40°C, time taken of 0.5‐48 hours, and stirring speed of 500‐1000rmp. It was discovered that magnetic stirring enhances the production of •OH, O2•, and h+ by the nanomaterials that are mechanistically responsible for the degradation of the dye pollutants. Also, it was revealed that expended tribocatalyst can be eluted mostly using H2O and can be reused up to 3–10 times while still sustaining degradation efficiency of >80% in most cases and this suggests the industrial scalability and eco‐friendliness potential of this approach.ConclusionIn the end, challenges and research gaps that can pave the way for method improvement and also serve as future research hotspots for researchers were presented.

In-situ synthesis of sunlight-driven CuO-ZnO heterostructure photocatalyst for enhanced elimination of organic pollutants and CO2 reduction

Removing hazardous organic pollutants, such as 4-nitrophenol (4-NP) and Congo red (CR) dyes from aqueous media and CO2 from the atmospheric medium remains a significant challenge. Herein, we report a facile in-situ synthetic approach for fabricating CuO-ZnO heterostructure photocatalysts through the surfactant-assisted co-precipitation method. The catalytic results demonstrate that the Cu1O-ZnO photocatalyst exhibits excellent activity under direct sunlight irradiation, owing to the heterostructure formation between the CuO and ZnO. The Cu1O-ZnO photocatalyst showed higher reaction rate constant (k) values of 0.20 min−1 for 4-NP and 0.09 min−1 for CR compared to previous reports. Additionally, efficient CO2 reduction was also achieved over Cu1O-ZnO photocatalyst. The optical and structural characterization results indicate that the improved photocatalytic reduction and degradation observed for the Cu1O-ZnO photocatalyst can be attributed to the strong synergistic interaction between p-type CuO and n-type ZnO and the construction of the p-n heterojunction. As a result, the absorption of visible light distinctly increased and inhibited the recombination rate of the photo-created electron-hole (e−/h+). Furthermore, the Cu1O-ZnO photocatalyst exhibited remarkable durability and recyclability, retaining high photoactivity (≥ 93%) after five cycles, demonstrating its potential for real-world applications in the photocatalytic reduction and degradation reactions under direct sunlight irradiation.

Surface methodology for optimized adsorption of hazardous organic pollutant from aqueous solutions via novel magnetic metal organic framework: Kinetics, isotherm study, and DFT calculations

An efficient way to remove Janus Green B (JGB) dye from contaminated water sources is using of magnetic cerium (III) metal–organic framework (MCe-MOF). Analytical methods such as PXRD, TEM, FESEM, FT-IR, PZC, and XPS were used in the characterization of the MCe-MOF microspheres in order to assess the phase, crystallinity, shape, surface characteristics, and chemical composition of the MCe-MOF material. Impressive physical characteristics of the synthesized MCe-MOF material included a high surface area of 1340.05 m2/g. Conversely, MCe-MOF’s magnetic saturation (MS) was measured at 36.47 emu.g−1. The purpose of the study was to determine if MCe-MOF could effectively remove JGB dye from wastewater by adsorption. Adsorption settings that were studied included pH, adsorbent dose, beginning dye concentration, contact time, and temperature. The JGB electrical characteristics, reactivity, and shape were ascertained through the application of density functional theory (DFT). The placement of electrophilic and nucleophilic attack sites is in good agreement with the molecular orbitals (HOMO and LUMO) and MEP results, according to DFT. Based on the findings, MCe-MOF had a high capacity for adsorbing JGB dye, with an adsorption data fit by pseudo-second-order kinetic models and the Langmuir isotherm. It was evident from the adsorption energy of 27.8 kJ.mol−1 that chemisorption was the mode of adsorption. The optimal conditions for attaining a high adsorption capacity were found to be pH 8 and 0.02 g of MCe-MOF dose. The adsorption process of JGB dye onto MCe-MOF was seen to be spontaneous, endothermic, and random, as indicated by the temperature-dependent increases in the thermodynamic parameters ΔGo, ΔHo, and ΔSo. The adsorption process was optimized through the application of Response Surface Methodology and Box-Behnken design (RSM, BBD). The successful removal of dyes from the MCe-MOF material was made possible by these methods. While π-π bonding happens through the interaction of aromatic rings, chemisorption entails the formation of chemical interactions between the adsorbate and adsorbent. Electrostatic interactions arise from the attraction or repulsion of charges between the adsorbate and adsorbent, and pore-filling happens when the adsorbate fills the adsorbent’s pores. For the removal of JGB dye from wastewater, MCe-MOF exhibits great potential as an adsorbent because of its numerous adsorption processes and high adsorption capacity.