Catalase activity as a diagnostic indicator of the health of oil-contaminated soils after remediation.

The work objective was to assess the ecological state of soils by changing the residual oil content and restoring catalase activity after remediation. The soils were selected in various ecosystems: a steppe of the Rostov Region (Haplic Chernozem), beech-hornbeam forests in the Republic of Adygea (Haplic Cambisols), and semi-desert of the Caspian province of the Republic of Kalmykia (Eutric Cambisols). Soil samples were polluted with oil at a concentration of 5% of the soil mass. After that, ameliorants (biochar, nitroammophoska, sodium humate, and Baikal EM-1) were introduced into the oil-contaminated soil. The catalase activity of Haplic Cambisols was stimulated only with the introduction of D2 biochar by 11% relative to the control, and in Haplic Chernozem, catalase was most stimulated with the addition of nitroammophoska D0.5 and D1 by 65% and 57% of the control, respectively. Nitroammophoska in all doses significantly stimulated the enzymatic activity, in Eutric Cambisols by four to six times compared to the control. The range of soil stability determined by catalase activity: Eutric Cambisols > Haplic Chernozem > Haplic Cambisols. Thus, it is most effective to apply biochar in doses of D and D2 and D0.5 and D nitroammophoska during the remediation of oil-contaminated Haplic Chernozem. For the remediation of Haplic Cambisols, it is effective to introduce biochar in dose of D2, and Eutric Cambisols-biochar and sodium humate in dose of D0.5 and nitroammophoska (all doses). The results of the study allow using catalase activity as a very informative and statistically significant diagnostical indicator of the health of oil-contaminated soils after remediation.

Nutrient depletion and heat stress impair the assimilation of nitrogen compounds in a scleractinian coral.

Concentrations of dissolved nitrogen in seawater can affect the resilience of the cnidarian-dinoflagellate symbiosis to climate change-induced bleaching. However, it is not yet known how the assimilation and translocation of the various nitrogen forms change during heat stress, nor how the symbiosis responds to nutrient depletion, which may occur due to increasing water stratification. Here, the tropical scleractinian coral Stylophora pistillata, in symbiosis with dinoflagellates of the genus Symbiodinium, was grown at different temperatures (26°C, 30°C and 34°C), before being placed in nutrient-replete or -depleted seawater for 24 h. The corals were then incubated with 13C-labelled sodium bicarbonate and different 15N-labelled nitrogen forms (ammonium, urea and dissolved free amino acids) to determine their assimilation rates. We found that nutrient depletion inhibited the assimilation of all nitrogen sources studied and that heat stress reduced the assimilation of ammonium and dissolved free amino acids. However, the host assimilated over 3-fold more urea at 30°C relative to 26°C. Overall, both moderate heat stress (30°C) and nutrient depletion individually decreased the total nitrogen assimilated by the symbiont by 66%, and combined, they decreased assimilation by 79%. This led to the symbiotic algae becoming nitrogen starved, with the C:N ratio increasing by over 3-fold at 34°C, potentially exacerbating the impacts of coral bleaching.

Optimization of Electrochemical Sensitivity in Anticancer Drug Quantification through ZnS@CNS Nanosheets: Synthesis via Accelerated Sonochemical Methodology.

Zinc sulfide/graphitic Carbon Nitride binary nanosheets were synthesized by using a novel sonochemical pathway with high electrocatalytic ability. The as- obtained samples were characterized by various analytical methods such as Transmission Electron Microscopy (TEM), Field emission scanning electron microscopy (FESEM), Energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction analysis (XRD), and X-ray photoelectron spectroscopy (XPS) to evaluate the properties of ZnS@CNS synthesized by this new route. Subsequently, the electrical and electrochemical performance of the proposed electrodes were characterized by using EIS and CV to establish an electroactive ability of the nanocomposites. The complete properties like structural and physical of ZnS@CNS were analyzed. As-prepared binary nanocomposite was applied towards the detection of anticancer drug (flutamide) by various electrochemical methods such as cyclic voltammetry (CV), differential pulse voltammetry (DPV) and amperometry. The glassy carbon electrode modified with a ZnS@CNS composite demonstrates a remarkable electrocatalytic efficiency for detecting flutamide in a pH 7.0 (PBS). The composite modified electrode shows synergistic effect of ZnS and CNS catalyst. The electrochemical sensing performance of the linear range was improved significantly due to high electroactive sites and rapid electron transport pathways. Crucially, the electrochemical method was successfully demonstrated in biological fluids which reveals its potential real-time applicability in the analysis of drug.

Synergistically Enhanced Electrochemical Sensing of Food Adulterant in Milk Sample at Erbium Vanadate/Graphitic Carbon Nitride Composite.

Dimetridazole (DMZ), a nitroimidazole derivative, is a notable antibiotic that has garnered growing interest in the medical community owing to its noteworthy pharmacological and toxicological properties. Increasing interest is being directed toward developing high-performance sensors for continuous monitoring of DMZ in food samples. This research investigated an electrochemical sensor-based nano-sized ErVO4 attached to a sheet-like g-CN-coated glassy carbon electrode to determine dimetridazole (DMZ). The chemical structure and morphological characterization of synthesized ErVO4@g-CN were analyzed with XRD, FTIR, TEM, and EDS. Irregular shapes of ErVO4 nanoparticles are approximately 15 nm. Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were followed to examine the electrochemical performance in pH 7 phosphate buffer solution for higher performance. This electrochemical sensor showed a low detection limit (LOD) of 1 nM over a wide linear range of 0.5 to 863.5 µM. Also, selectivity, stability, repeatability, and reproducibility studies were investigated. Furthermore, this electrochemical sensor was applied to real-time milk sample analysis for the detection of analytes.

CDs-g-C3N4-oleaginous yeast hybrid system: Microbial lipid synthesis and fermentation residual reutilization.

The utilization of solar energy and fast-growing heterotrophic microbes for biofuel production has been recognized as a promising approach to achieve carbon neutrality and address energy crisis. In this work, we synthesized different kinds of photocatalysts based on graphitic carbon nitride (g-C3N4). We found that carbon dots modified-graphitic carbon nitride (CDs-g-C3N4) showed the highest photocatalytic activity. Subsequently, we developed a photocatalyst-microbe hybrid (PMH) system by combining CDs-g-C3N4 with an oleaginous yeast strain, Cutaneotrichosporon dermatis ZZ-46. Under visible light irradiation, the lipid yield of this PMH system reached 1.70 g/L at 120 h, representing a 36 % increase compared to the control. The photocatalytic reaction-induced ROS and the reductive photogenerated electrons facilitated ZZ-46 cells to synthesize more lipids. Furthermore, the fermentation residual of this PMH system was reutilized to prepare biochar via pyrolysis. The biochar generated at 550 °C (BC-550) demonstrated exceptional adsorption capabilities, particularly with a 57 % adsorption rate for methylene blue (MB), and maintained its perfect adsorption efficacy even after five regeneration cycles. These results offer promising avenues for addressing energy shortages and environmental contamination.

Light harvesting enhancement through band structure engineering in graphite carbon nitride / polydopamine nanocomposite photocatalyst: Addressing persistent organophosphorus pesticide pollution in water systems.

Organophosphorus pesticides, particularly profenofos (PF), pose a significant threat to the food supply and human health due to their persistence, toxicity, and resistance to natural breakdown processes. An urgent need exists for an environmentally friendly solution, and photocatalysis emerges as a practical, cost-effective option. However, challenges like poor light responsiveness and difficulties in material separation and reusability persist. To address these issues, we developed a nanocomposite consisting of graphite carbon nitride (g-C3N4) doped with polydopamine (pDA) through a hydrothermal synthesis method. This innovative nanocomposite was employed as a photocatalyst to degrade PF. Various analytical techniques, including UV-DRS, FT-IR, XRD, HR-TEM, and EDAX, were utilized to characterize the synthesized nanocomposite. The strategically modulated band gaps of the nanocomposite enable efficient absorption of UV light, facilitating the robust photocatalytic degradation of PF (96.4%). Our study explored photodegradation using different g-C3N4/pDA catalyst dosages, varied PF concentrations, and pH levels (3, 5, 9, and 11) under UV light. Our findings promise applications in wastewater management, offering an efficient catalyst for PF degradation. This marks a significant stride in addressing challenges related to pesticide pollution in the environment.

ZIF-67 based CoS2 self-assembled on graphitic carbon nitride microtubular for sensitive electrochemical detection of paraquat in fruits.

Paraquat (PQ) is a widely used and harmful herbicide that must be detected in the environment. This study reports a novel composite (CoS2-GCN) prepared by assembling cobalt disulfide (CoS2) derived from metal-organic frameworks (MOFs) on graphitic carbon nitride (GCN). An electrochemical sensor (CoS2-GCN/ glassy carbon electrode (GCE)) was successfully prepared by modifying CoS2-GCN onto a GCE to sensitively detect PQ. Different concentrations of PQ were detected using square-wave voltammetry, and the CoS2-GCN/GCE electrochemical sensor showed remarkable response signals for PQ in the range of 20 - 1000 nM and 1 - 13 µM, with a detection limit of 4.13 nM (S/N = 3). The CoS2-GCN/GCE electrochemical sensor exhibited high stability, reproducibility, and immunity to interference, which were attributed to the synergistic effects of CoS2 and GCN. In addition, the CoS2-GCN/GCE electrochemical sensor showed high applicability for the analysis of fruit samples. Therefore, the proposed sensor has potential applications in PQ detection.

Improved photocatalytic oxidation of micropollutant in wastewater by solar light: assisted palladium-doped graphitic carbon nitride.

The escalating global industrial expansion has led to the extensive release of organic compounds into water bodies, resulting in substantial pollution and posing severe threats to both human health and the ecosystem. Among common micropollutants, bisphenol A (MP-BA) has emerged as a significant endocrine-disrupting chemical with potential adverse effects on human health and the environment. This study aims to develop an efficient photocatalyst, specifically by incorporating palladium-doped graphitic carbon nitride (Pd@GCN), to eliminate MP-BA pollutants present in industrial wastewater. The examination of optical properties and photoluminescence indicates that incorporating Pd into GCN enhances the visible light absorption spectra, which extends beyond 570 nm, and accelerates the separation rate of electron-hole pairs. The photocatalytic degradation efficiency of MP-BA increases from 81.7 to 98.8% as the solution pH rises from 5.0 to 9.0. Moreover, Pd@GCN significantly improves the removal rate of MP-BA in wastewater samples, reaching an impressive 92.8% after 60 min of exposure to solar light. Furthermore, the Pd@GCN photocatalyst exhibits notable reusability over six cycles of MP-BA degradation, indicating its promising potential for the treatment of organic pollutants in wastewater under solar light conditions.

Layer-by-layer assembled graphitic carbon nitride membranes for water treatment.

Meeting societal demand for potable water supply remains one of the prioritized challenges faced in the modern era. The anthropogenic intervention has led to a dire situation threatening ecological balance and human health. There is an inevitable need for the development of new technologies and innovations in existing technologies for water treatment. Photocatalytic Membrane technology, encompassing the merits of membrane filtration and photocatalytic degradation has evolved as a potential and reliable technology for sustainable water treatment. Innovations in photocatalytic materials and membrane fabrication techniques can lead to the goal of commercialization of membrane water treatment technology. Herein, we demonstrate the potential of graphitic carbon nitride (g-C3N4) and its functionalized analog as photocatalytic membranes for sustainable water treatment. g-C3N4 and Tetracarboxyphenylporphyrin sensitized g-C3N4 (g-C3N4/TCPP) was introduced onto commercial nylon membrane surface via a layer-by-layer (LBL) assembly method using chitosan and sodium salt of polystyrene sulphonic acid as polyelectrolytes. The fabricated membranes were characterized to ensure the integration of the photocatalysts. The performance of the membranes for water treatment was assessed by selecting some common dyes as model pollutants. The modified membranes exhibited excellent flux recovery and could afford high rejection rates upon irradiation indicating the prospects for sustainable filtration.

Electrochemical Nanoaptasensor Based on Graphitic Carbon Nitride/Zirconium Dioxide/Multiwalled Carbon Nanotubes for Matrix Metalloproteinase-9 in Human Serum and Saliva.

In this study, a nanocomposite was synthesized by incorporating graphitic carbon nanosheets, carboxyl-functionalized multiwalled carbon nanotubes, and zirconium oxide nanoparticles. The resulting nanocomposite was utilized for the modification of a glassy carbon electrode. Subsequently, matrix metalloproteinase aptamer (AptMMP-9) was immobilized onto the electrode surface through the application of ethyl-3-(3-(dimethylamino)propyl)carbodiimide hydrochloride-N-hydroxysuccinimide (EDC-NHS) chemistry. Morphological characterization of the nanomaterials and the nanocomposite was performed using field-emission scanning electron microscopy (FESEM). The nanocomposite substantially increased the electroactive surface area by 205%, facilitating enhanced immobilization of AptMMP-9. The efficacy of the biosensor was evaluated using cyclic voltammetry (CV) and differential pulse voltammetry (DPV). Under optimal conditions, the fabricated sensor demonstrated a broad range of detection from 50 to 1250 pg/mL with an impressive lower limit of detection of 10.51 pg/mL. In addition, the aptasensor exhibited remarkable sensitivity, stability, excellent selectivity, reproducibility, and real-world applicability when tested with human serum and saliva samples. In summary, our developed aptasensor exhibits significant potential as an advanced biosensing tool for the point-of-care quantification of MMP-9, promising advancements in biomarker detection for practical applications.

Photoluminescent Self-Healable Waterborne Polyurethane/Mo and S Codoped Graphitic Carbon Nitride Nanocomposite with Bioimaging and Encryption Capability.

Creating polymers that combine various functions within a single system expands the potential applications of such polymeric materials. However, achieving polymer materials that possess simultaneously elevated strength, toughness, and self-healing capabilities, along with special properties, remains a significant challenge. The present study demonstrates the preparation of S and Mo codoped graphitic carbon nitride (g-C3N4) (Mo@S-CN) nanohybrid and the fabrication of self-healing waterborne polyurethane (SHWPU)/Mo@S-CN (SHWPU/NS) nanocomposites for advanced applications. Mo@S-CN is an intriguing combination of g-C3N4 nanosheets and molybdenum oxide (MoOx) nanorods, forming a complex lamellar structure. This unique arrangement significantly improves the inborn properties of SHWPU to an impressive degree, especially mechanical strength (28.37-34.11 MPa), fracture toughness (73.65-140.98 MJ m-2), and thermal stability (340.17-348.01 °C), and introduces fluorescence activity into the matrix. Interestingly, a representative SHWPU/NS0.5 film is so tough that a dumbbell of 15 kg, which is 53,003 times heavier than the weight of the film, can be successfully lifted without any significant crack. Remarkably, fluorescence activity is developed because of electronic excitations occurring within the repeating polymeric tris-triazine units of the Mo@S-CN nanohybrid. This fascinating feature was effectively harnessed by assessing the usability of aqueous dispersions of the Mo@S-CN nanohybrid and photoluminescent SHWPU/NS nanocomposites as sustainable stains for bioimaging of human dermal fibroblast cells and anticounterfeiting materials, respectively. The in vitro fluorescence tagging test showed blue emission from 365 nm excitation, green emission from 470 nm excitation, and red emission from 545 nm excitation. Most importantly, in vitro hemocompatibility assessment, in vitro cytocompatibility, cell proliferation assessment, and cellular morphology assessment supported the biocompatibility nature of the Mo@S-CN nanohybrid and SHWPU/NS nanocomposites. Thus, these materials can be used for advanced applications including bioimaging.

Synergistic effect of adsorption and photocatalytic degradation of oilfield-produced water by electrospun photocatalytic fibers of Polystyrene/Nanorod-Graphitic carbon nitride.

Graphitic carbon nitride with nanorod structure (Nr-GCN) was synthesized using melamine as a precursor without any other reagents by hydrothermal pretreatment method. XRD, FTIR, SEM, N2 adsorption-desorption from BET, UV-Vis DRS spectroscopy, and photoluminescence were used to characterize the prepared samples. Also, the photoelectrochemical behavior of nanoparticles was studied by photocurrent transient response and cyclic voltammetry analysis. Polystyrene (PS) fibrous mat was fabricated by electrospinning technique and used as a support for the stabilization of the nanoparticles. The performance of the synthesized nanoparticles and photocatalytic fibers (PS/Nr-GCN) was evaluated in oilfield-produced water treatment under visible light irradiation. During this process, oil contaminants were adsorbed by hydrophobic polystyrene fibers and simultaneously degraded by Nr-GCN. The removal efficiency of chemical oxygen demand (COD) has been obtained 96.6% and 98.4% by Nr-GCN and PS/Nr-GCN, respectively, at the optimum conditions of pH 4, photocatalyst dosage 0.5 g/L, COD initial concentration 550 mg/L, and illumination time 150 min. The gas chromatography-mass spectroscopy analysis results showed 99.3% removal of total petroleum hydrocarbons using photocatalytic fibers of PS/Nr-GCN. The results demonstrated that the GCN has outstanding features like controllable morphology, visible-light-driven, and showing high potential in oily wastewater remediation. Moreover, the synergistic effect of adsorption and photocatalytic degradation is an effective technique in oilfield-produced water treatment.

Graphitic-carbon-nitride-hydrophilicity-dependent photocatalytic degradation of antibiotics with different log Kow.

The surface hydrophilicity of a photocatalyst is an important factor that directly influences its interactions with organic pollutants and significantly impacts its degradation. In this study, we investigated the impact of increased hydrophilicity of g-C3N4 (CN) by alkaline solvothermal treatment on the degradations of three antibiotics (oxytetracycline (OTC), oxolinic acid (OA), and sulfamethoxazole (SMX)) with different log Kow values. Scanning electron microscopy (SEM), X-ray diffraction analysis (XRD), and Fourier-transform infrared (FT-IR) spectroscopy showed no significant differences in the morphology, crystalline structure, and surface functional groups of CN after alkaline solvothermal treatment (Nv-HPCN). However, contact angle analysis revealed that Nv-HPCN (31.8°) was more hydrophilic than CN (61.1°). To assess the hydrophilicity of the antibiotics, the log Kow values of SMX (0.77), OA (0.43), and OTC (-0.34) were measured. Nv-HPCN showed faster OTC degradation than CN, whereas the opposite pattern was observed for the degradation of OA. Scavenger tests showed that O2•- and h+ mainly contributed to the degradation of these antibiotics. Furthermore, the influences of NOM and coexisting anions on antibiotic degradation were investigated. This study thus offers perspectives on the impact of surface hydrophilicity of photocatalysts on the degradation of antibiotics.

Microbial lipid synthesis based on visible light-driven oxygen doped-graphitic carbon nitride /oleaginous yeast hybrid system.

The use of solar energy and heterotrophic microbes to synthesize microbial lipids is a promising strategy to solve energy crisis and reduce CO2 emissions. In this study, a photocatalyst, oxygen-doped graphitic carbon nitride (O-g-C3N4), was synthesized and combined with an oleaginous yeast strain, Cutaneotrichosporon dermatis ZZ-46, to construct a photocatalyst-microbe hybrid (PMH) system. Under illumination, the lipid yield of the PMH system reached 1.61 g/L after 96 h (87 % higher than that of control). NADPH/NADP+ ratio of ZZ-46 cells in the PMH system increased. Metabolomics results revealed that glutathione generation was increased, and the fatty acid decomposition pathway in ZZ-46 cells was inhibited in the PMH system. This study provides a new approach for the synthesis of microbial lipids based on solar energy and heterotrophic microbes.

Two-dimensional heterojunction layered graphene oxide/graphitic carbon nitride photocatalyst for removal of toxic environmental dye methylene blue.

The direct thermal polymerization techniques were applied to prepare the graphene oxide (GO)-graphitic carbon nitride (gCN) hybrid structure. The prepared hybrid heterojunction GO-gCN nanosheets were utilized as a photocatalyst to remove model pollutants methylene blue (MB) dye. The basic physio-chemical properties of GO-gCN layered materials have been analyzed by various characterization techniques. In addition, the proposed materials have a higher photocatalytic ability toward the degradation of aqueous solution of MB dye under visible light irradiation within a short treatment time. This is because it's the synergistic effects of GO-gCN layer-by-layer structures produced by π─π stacking with charge-transfer interactions. The gCN with GO composite can able to enhance the charge transfer and light-harvesting properties. Under the influence of photocatalyst, the surface of Graphene oxide undergoes the separation and combination of carbonyl radicals, hydroxyl radicals, epoxy radicals, and electron-hole pairs. This enhances the absorption of visible light and improves the degradation of MB, when GO is incorporated into gCN. The removal efficiency of MB reached up to 82.311% within the short treatment time.

Benzopyrene elimination from the environment using graphitic carbon nitride-SnS nanocomposites.

Benzopyrene (BaP) stands as a potent polycyclic aromatic hydrocarbon (PAH) molecule, boasting five fused aromatic rings, making its way into the human food chain through soil contamination. The persistent environmental presence of PAHs in soil, attributed to industrial exposure, is primarily due to their low molecular weight and hydrophobic nature. To preemptively address the entry of BaP into the food chain, the application of nanocomposites was identified as an effective remediation strategy. Post-synthesis, comprehensive characterization tests employing techniques such as UV-DRS, XRD, SEM-EDX, FTIR, and DLS unveiled the distinctive features of the g-C3N4-SnS nanocomposites. These nanocomposites exhibited spherical shapes embedded on layers of nanosheets, boasting particle diameters measuring 88.9 nm. Subsequent tests were conducted to assess the efficacy of eliminating benzopyrene from a combination of PAH molecules and g-C3N4-SnS nanocomposites. Varied parameters, including PAH concentration, adsorbent dosage, and suspension pH, were systematically explored. The optimized conditions for the efficient removal of BaP utilizing the g-C3N4-SnS nanocomposite involved 2 µg/mL of benzopyrene, 10 µg/mL of the nanocomposite, and a pH of 5, considering UV light as the irradiation source. The investigation into the mechanism governing BaP elimination closely aligned with batch adsorption results involved a thorough exploration of adsorption kinetics and isotherms. Photocatalytic degradation of benzopyrene was achieved, reaching a maximum of 86 % in 4 h and 36 % in 2 h, with g-C3N4-SnS nanocomposite acting as the catalyst. Further validation through HPLC data confirmed the successful removal of BaP from the soil matrix.

Improving U(VI) retention efficiency and cycling stability of GCN-supported calcined-LDH composite: Mechanism insight and real water system applications.

The synthesis and characterization of graphitic carbon nitride (GCN) and its composites with calcined layered double hydroxide (CLDH) were examined in this investigation. The goal was to assess these composites' maximum adsorption capacity (qmax) for U(VI) ions in wastewater. Several different characterization methodologies were utilized to examine the fabricated substances. These methods encompass X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The GCN-CLDH composite displayed enhanced adsorption ability towards U(VI) ions due to its high surface functionality. Langmuir adsorption isotherm analysis showed that more than 99% of U(VI) ions were adsorbed, with a qmax of 196.69 mg/g. The kinetics data exhibited a good fit for a pseudo-second-order (PSO) model. Adsorption mechanisms involving precipitation and surface complexation via Lewis's acid-base interactions were proposed. The application of the GCN-CLDH composite in groundwater demonstrated adsorption below the maximum permissible limit established by USEPA, indicating improved cycling stability. These observations underscore the capacity of the GCN-CLDH composite's proficiency in adsorbing U(VI) aqueous solutions containing radioactive metals.

Enhanced antibiotic degradation via photo-assisted peroxymonosulfate over graphitic carbon nitride nanosheets/CuBi2O4: Highly efficiency of oxygen activation and interfacial charge transfer.

Improving the activation capacity of peroxymonosulfate (PMS) to increase radical and non-radical production is critical for antibiotic degradation. However, how to boost reactive oxygen species (ROS) and speed interfacial charge transfer remains an essential challenge. We report a coupling system of 10 %CNNS/CuBi2O4 photocatalyst and sulfate radical-based advanced oxidation processes (SO4--AOPs) to enhance the activation of PMS and improve antibiotic degradation. Owing to highly efficient oxygen activation and interfacial charge transfer, the degradation efficiency of the photo-assisted PMS system was as high as 51.6 times and 2.8 times that of photocatalyst and SO4--AOPs alone, respectively. Importantly, the highly efficient oxygen activation resulted in the production of O2-, which in turn could utilize the excess electrons generated through efficient interfacial charge transfer to convert into non-radical 1O2. The total organic carbon (TOC) elimination effectiveness of the photo-assisted PMS system reached 82 % via the synergy of radicals and non-radicals (O2-, OH, 1O2, SO4-, h+). This system also had excellent potential for reducing the generation and toxicity of disinfection by-products (DBPs), as evidenced through significant reductions in concentrations of trichloromethane (TCM), dichloroacetic acid (DCAA), and trichloronitromethane (TCNM) by 76 %, 64 %, and 35 %, respectively, providing an effective and eco-friendly strategy for antibiotic treatment.

Fabrication of UiO-66/GCN, a Hybrid Photocatalyst, for Effective Degradation of Ciprofloxacin, Toxicity Estimation, and Its Antibacterial Activity.

Fabrication of a metal-organic framework-based photocatalyst has been gaining much interest due to its higher surface area and reasonable band gap, enhancing its photocatalytic activity. This study attempted a facile synthesis of the hybrid photocatalyst UiO-66 doped with graphitic carbon nitride (GCN) by a simple solvothermal method. This composite minimized the drawback related to photogenerated charge transfer and recombination and helped the absorption of visible light. The material was investigated by using various instrumental techniques. In this work, ciprofloxacin (CIP), a fluoroquinolone drug, was chosen as a target micropollutant, and a photodegradation experiment was carried out by using UiO-66, GCN, and UiO-66/GCN under a visible light source, which exhibited 81.85, 69.48, and 93.60% of degradation, respectively. Finally, liquid chromatography mass spectrometry analysis and theoretical computation were carried out to identify the CIP degradation mechanism, and T.E.S.T. software was used to investigate the toxicity of the intermediate products. Apart from photocatalytic activity, the prepared material was also tested for its antibacterial properties against Staphylococcus aureus and Escherichia coli.

Promoting the suitability of graphitic carbon nitride and metal oxide nanoparticles: A review of sulfonamides photocatalytic degradation.

The widespread consumption of pharmaceutical drugs and their incomplete breakdown in organisms has led to their extensive presence in aquatic environments. The indiscriminate use of antibiotics, such as sulfonamides, has contributed to the development of drug-resistant bacteria and the persistent pollution of water bodies, posing a threat to human health and the safety of the environment. Thus, it is paramount to explore remediation technologies aimed at decomposing and complete elimination of the toxic contaminants from pharmaceutical wastewater. The review aims to explore the utilization of metal-oxide nanoparticles (MONPs) and graphitic carbon nitrides (g-C3N4) in photocatalytic degradation of sulfonamides from wastewater. Recent advances in oxidation techniques such as photocatalytic degradation are being exploited in the elimination of the sulfonamides from wastewater. MONP and g-C3N4 are commonly evolved nano substances with intrinsic properties. They possessed nano-scale structure, considerable porosity semi-conducting properties, responsible for decomposing wide range of water pollutants. They are widely applied for photocatalytic degradation of organic and inorganic substances which continue to evolve due to the low-cost, efficiency, less toxicity, and more environmentally friendliness of the materials. The review focuses on the current advances in the application of these materials, their efficiencies, degradation mechanisms, and recyclability in the context of sulfonamides photocatalytic degradation.