Organic Pollutants In Aquatic Environment Research Articles

Intraplanar heterostructure-mediated activation of peroxydisulfate for singular-electron-transfer degradation of organic pollutants

Activating peroxydisulfate (PDS) through electron transfer pathways (ETP) is promising for degrading organic pollutants in aquatic environments. However, enhancing the activation selectivity remains a challenge. Herein, this study developed an intraplanar heterojunction with C-ring grafted g-C3N4 (CCN) as the catalyst, enabling PDS activation through a singular ETP. The CCN/PDS system achieved complete degradation and efficient mineralization (87.15 %) of bisphenol F (BPF), significantly reducing its ecological toxicity. Both experimental and theoretical investigations revealed that the intraplanar heterojunction could modulate the orbital occupation in g-C3N4/PDS, enhancing PDS adsorption and activation selectivity. Driven by the differences in the frontier orbital energy, the CCN/PDS system achieved a singular ETP without active species formation. The CCN/PDS system efficiently degraded BPF in complex water environments, showing performance stability across a wide pH range and against various coexisting ions. In a continuous-flow automatic catalytic device, the CCN/PDS system maintained a constant 100 % BPF degradation for 600 min. This study advances the understanding of PDS activation via singular ETP and introduces a new approach to water purification.

Natural Vanadium–Titanium Magnetite Activated Peroxydisulfate and Peroxymonosulfate for Acid Orange II Degradation: Different Activation Mechanisms and Influencing Factors

Persulfate-based advanced oxidation processes have emerged as a promising approach for the degradation of organic pollutants in aqueous environments due to their ability to generate sulfate radicals (SO4−·) within catalytic systems. In this study, peroxydisulfate (PDS) and peroxymonosulfate (PMS) were investigated with the natural vanadium–titanium magnetite (VTM) as the activator for the degradation of acid orange II. The degradation efficiency increased with higher dosages of VTM or persulfate (both PDS and PMS) at lower concentrations (below 10 mM). However, excessive PMS (higher than 10 mM) in the PMS/VTM system led to the self-consumption of free radicals, significantly inhibiting the degradation of acid orange II. The VTM-activated PDS or PMS maintained an effective degradation of acid orange II in a wide pH range (3~11), suggesting remarkable pH stability. The SO4−· was the main active species in the PDS/VTM system, while hydroxyl radical (·OH) also contributed significantly to the PMS/VTM system. In addition, PMS exhibited better thermal stability during VTM activation. Coexisting ions in an aqueous environment such as bicarbonate (HCO3–), carbonate (CO32–), and hydrogen phosphate (HPO42–) had obvious effects on persulfate activation. Our study systematically investigated the different activation processes and influencing factors associated with PDS and PMS when the natural VTM was used as a catalyst, thereby providing new insights into the persulfate-mediated degradation of organic pollutants in aqueous environments.

Innovative fabrication of highly efficient CeO2 ceramic nanomaterials for enhanced photocatalytic degradation of toxic contaminants under sunlight

In this research, we report an innovative sonochemical technique for synthesizing cerium oxide (CeO2) nanoparticles utilizing glucose as a capping agent, significantly boosting their photocatalytic performance under visible light. Through meticulous optimization, our CeO2 nanoparticles demonstrated exceptional degradation efficiencies: 97.2 % for Acid Red 14, 99.1 % for Captopril, 98.7 % for Malachite Green, and 98.3 % for Amlodipine, substantially outstripping performance metrics of commercial TiO2 and untreated samples. Our kinetic analyses, based on the Langmuir-Hinshelwood model, indicated a superior rate constant of 0.0701 min⁻1 for Acid Red 14 degradation—reflecting a stark enhancement over other catalysts tested. Furthermore, mechanistic insights revealed that the significant improvement in photocatalytic activity was predominantly due to the generation of hydroxyl radicals and effective utilization of electron vacancies, with the role of these reactive species validated by detailed scavenger tests. This enhancement in photocatalytic efficiency is attributed to the sonochemical synthesis paired with glucose modification, which optimizes the nanoparticles' surface characteristics crucial for reactivity. Moreover, the nanoparticles showcased remarkable stability and reusability, maintaining an 87.8 % degradation rate after 11 cycles, evidencing minimal loss in activity and underscoring their potential for long-term applications in environmental remediation. This study not only paves the way for the practical application of CeO2 nanoparticles in pollutant degradation but also illustrates the broader applicability of sonochemically synthesized nanomaterials in sustainable environmental management, offering a promising solution to the challenge of complex organic pollutants in aquatic environments.

Effect of PCBs on Production Characteristics and Fucoxanthin / Fatty Acid Content of Cylindrotheca closterium (Ehrenberg) Reimann et Lewin Diatom Enrichment Culture

Background: Since the mid-20th century, polychlorinated biphenyls (PCBs) have emerged as one of the foremost anthropogenic organic pollutants in aquatic environments. Microphytobenthic algae of the genus Cylindrotheca have been recurrently employed in laboratory experiments to assess sediment toxicity. Recently, a novel strain of benthic diatoms belonging to the genus Cylindrotheca has been identified and characterized from PCB-contaminated sediments in the coastal region of Sevastopol Bay (Black Sea). This species of algae has high biomass productivity, the ability to synthesize fucoxanthin, and a variety of fatty acids. Cylindrotheca closterium is capable of metabolizing organic pollutants in bottom sediments. Objective: The objective of the study was to investigate the effects of PCBs on the growth patterns and physiological responses of C. closterium through a 9-day experiment, subjecting the microalgae to varying concentrations of PCBs ranging from 0.0003 to 100 mg/L. Results: The experiments revealed that C. closterium could grow in environments containing concentrations of PCBs ranging from 0.0003 to 10 mg/L, indicating its resilience to moderate levels of PCB exposure. Additionally, adaptive biochemical processes were observed in C. closterium under PCB exposure. Notably, on the sixth day of the experiment, the culture transitioned into a stationary growth phase, accompanied by significant increases in total lipid content by 1.6 times and fucoxanthin by 4.6 times compared to the control. However, a pronounced decrease in culture growth was observed at a PCB concentration of 100 mg/L, coinciding with reductions in total lipid and fucoxanthin content, suggesting a tolerance threshold of C. closterium between 10 and 100 mg/L PCB concentrations. Furthermore, alterations in the fatty acid profile of C. closterium were noted, characterized by a decrease in polyene content and an increase in monoene fatty acids, under PCB exposure. Conclusion: The study underscores the resilience of C. closterium to moderate PCB concentrations and highlights the complex physiological responses and adaptive mechanisms initiated in response to PCB exposure. The findings contribute to understanding the toxic effects of PCBs on C. closterium and provide insights into potential mechanisms underlying these effects.

Mineralization of clofibric acid by persulfate-promoted catalytic subcritical water oxidation process using CoFe2O4@SiO2 catalyst

The design and use of innovative treatment processes are very important in preventing the possible toxic effects of organic pollutants in aquatic environments. One of these methods is the subcritical water oxidation method, which has been used recently. In the current study, the mineralization of clofibric acid (CFA) was carried out under more effective and mild conditions using persulfate (PS) as an oxidant and CoFe2O4@SiO2 catalyst by the subcritical water oxidation (sub-CWO) process. Characterization of the synthesized catalyst was performed through XRD, FTIR, TEM and SEM–EDS analyses. In the CFA oxidation with persulfate-promoted catalytic Sub-CWO process, optimum working conditions was determined as 15 mM PS, 40 min, 383 K, and 0.3 g L−1 catalyst dosage using the response surface method and Box–Behnken design. The catalyst's efficiency remained relatively stable after three cycles under optimal conditions, resulting in a 97% total organic carbon (TOC) removal. Decomposition products were determined and a degradation mechanism was proposed.

Activated Periodates and Sodium Percarbonate in Advanced Oxidation Processes of Organic Pollutants in Aqueous Media: A Review

The methods of periodates and sodium percarbonate activation are considered for planning strategic approaches to increasing the efficiency and intensity of oxidative degradation of organic pollutants in aquatic environments. A classification of periodate activation methods is proposed, including activation methods by external energy effects, catalytic activation methods, and other activation methods (e.g., by hydrogen peroxide, by hydroxylamine, activation in alkaline medium). Activation methods for sodium percarbonate were divided into homogeneous and heterogeneous activation methods.

Cyano-deficient g-C3N4 for round-the-clock photocatalytic degradation of tetracycline: Mechanism and application prospect evaluation

Without light at night, the system for photocatalytic degradation of refractory organic pollutants in aquatic environments based on free radicals will fall into a dormant state. Hence, a round-the-clock photocatalyst (CCN@SMSED) was prepared by in situ growth of cyanide-deficient g-C3N4 on the surface of Sr2MgSi2O7:Eu2+,Dy3+ through a simple calcination method. The CCN@SMSED exhibits an outstanding oxidative degradation ability for refractory tetracycline (TC) in water under both light and dark conditions, which is attributed to the synergistic effect of free radical (•O2− and •OH) and non-radical (h+ and 1O2). Electrochemical analyses further indicate that direct electron transfer (DET) is also one of the reasons for the efficient degradation of TC. Remarkably, the continuous working time of the round-the-clock photocatalyst in a dark environment was estimated for the first time (about 2.5 h in this system). The degradation pathways of TC mainly include demethylation, ring opening, deamination and dehydration, and the growth of Staphylococcus aureus shows that the process is biosafe. More importantly, CCN@SMSED holds significant promise for practical application due to its low energy consumption and suitability for removing TC from a variety of complex water bodies. This work provides an energy consumption reference for the practical application of round-the-clock photocatalytic degradation of organic pollutants.

Synergistic Photocatalysis of Bayerite/Zeolite Loaded TiO2 Nanocomposites for Highly Efficient Degradation of Organic Pollutants in Aqueous Environments

Synergistic Photocatalysis of Bayerite/Zeolite Loaded TiO2 Nanocomposites for Highly Efficient Degradation of Organic Pollutants in Aqueous Environments

Self-powered organic pollutants degradation in wastewater by photocatalytic ozonation based on triboelectric nanogenerator

It is of great significance to explore innovative ways to degrade organic pollutants in wastewater. Here, for the first time, we report a self-powered photocatalytic ozonation water purification system for removing organic pollutants in aquatic environment. A rabbit fur-based rotary triboelectric nanogenerator (RR-TENG) is designed as the power supply of water purification system. As a new TENG-based ozone generation method, spark-surface dielectric barrier discharge (Spark-SDBD) is proposed, which is composed of spark discharge device and surface dielectric barrier discharge (SDBD) device in series and can generate ozone to a maximum concentration of 36.4 mg/m3. Rhodamine B and ciprofloxacin, two typical organic compounds, are selected as simulated pollutants in wastewater, and P25 particles loaded on nickel foam are used as the photocatalyst. Ozone is continuously introduced into the polluted solution through an aeration device, coupled with photocatalysis. Within 80 minutes, it can be observed that Rhodamine B has 100% decolorization and ciprofloxacin is degraded to 99%. This work broadens the field of water purification and provides an effective way to create a cleaner and safer aquatic environment.

Novel core-shell structural nZVI@Fe2P for sulfadiazine (SDZ) degradation: Accelerated Fe(III)/Fe(II) dynamic cycling, boosted Fenton performance and stability

Nano zero valent iron (nZVI) is widely used in traditional hydrogen peroxide (H2O2)-based Fenton reactions for the degradation of persistent organic pollutants in aqueous environments. How to restrain the blocked electron transfer aroused from thickening of the iron oxide passivation layer and reinforce the Fe(III)/Fe(II) dynamic cycling is essential for Fenton reactions. In this work, a novel core–shell structural nZVI@Fe2P was fabricated and employed for the degradation of sulfadiazine (SDZ). Compared to nZVI, the nZVI@Fe2P demonstrated a significant performance and stability in the degradation of SDZ. Completed SDZ removal is achieved in less than 15 min and the SDZ removal kept over 60% even in the ninth consecutive cycles. Although the SDZ removal decreased dramatically to only 27.4% in the tenth cycle, the value could be restored to 80.6% after a facile re-phosphorization process. Both experimental and density function theory (DFT) calculation revealed the dominant role of Fe2P in promoting H2O2 activation and strengthening the Fe(III)/Fe(II) dynamic cycling. In the nZVI@Fe2P/H2O2 system, the low impedance and high proton conductivity of the Fe2P shell layer played a dual function, i.e., accelerating electron transfer and donating electrons for the continuous Fenton reaction. This implication of these findings provides a novel strategy by integrating the state-of-the-art material science, advanced oxidation process, and mechanism elucidation for practical environmental wastewater remediation.

Development of diffusive gradients in thin-films technique for monitoring polycyclic aromatic hydrocarbons in coastal waters

Addressing the challenge of accurately monitoring polycyclic aromatic hydrocarbons (PAHs) in aquatic systems, this study employed diffusive gradients in thin-films (DGT) technique to achieve methods detection limits as low as 0.02 ng L−1 to 0.05 ng L−1 through in situ preconcentration and determination of time-integrated concentrations. The efficacy of the developed DGT samplers was validated under diverse environmental conditions, demonstrating independence from factors such as pH (5.03–9.01), dissolved organic matter (0–20 mg L−1), and ionic strength (0.0001–0.6 M). Notably, the introduction of a novel theoretical approach to calculate diffusion coefficients based on solvent-accessible volume tailored for PAHs significantly enhanced the method’s applicability, particularly for organic pollutants with low solubility. Field deployments in coastal zones validated the DGT method against traditional grab sampling, with findings advocating a 4 to 7-day optimal deployment duration for balancing sensitivity and mitigating lag time effects. These results provide a sophisticated, efficient solution to the persistent challenge of monitoring hydrophobic organic pollutants in aquatic environments, broadening the scope and applicability of DGT in environmental science and providing a robust tool for researchers.

Synthesis and photocatalytic activity of BiOI particles: An efficient visible-light-driven degradation of organic pollutants in aqueous environments

Bismuth oxyiodide (BiOI) particles were successfully fabricated through solvothermal activation using bismuth (III) nitrate pentahydrate and potassium iodide as precursors. The photocatalytic activities of BiOI were investigated under the influence of synthesis temperature (120–200 °C) with a fixed duration of 12 h. The physical-chemical properties of the samples were systematically investigated using X-ray diffraction, scanning electron microscopy, N2-sorption isotherm techniques, and pH of the point of zero charge (pHpzc). The prepared BiOI exhibited a single phase with a non-uniform 2D morphology with different sizes, an average crystallite size of 30 nm, and a BET surface area of 20.71 m²g−1. The zero-point charge was determined to be 7.7. The photocatalytic performance under simulated solar light irradiation was investigated by examining the effects of dye initial concentration, catalyst dose, and dye pH. Remarkably, BiOI synthesized at 160 °C demonstrated an impressive 85% removal efficiency of 10 ppm MO (methyl orange) at normal pH levels (pH 6.8) within 120 min under visible light irradiation, along with the highest rate constant of 0.01418 min−1. The quenching effects of different scavengers indicate the significant role of reactive O2•– and a minor role of hVB+ and •OHads in the photocatalytic process. These findings underscore the potential of BiOI particles as efficient photocatalysts for environmental applications, particularly in the degradation of organic pollutants in water using solar light irradiation.

Preparation of Cobalt-Nitrogen Co-Doped Carbon Nanotubes for Activated Peroxymonosulfate Degradation of Carbamazepine.

Cobalt-nitrogen co-doped carbon nanotubes (Co3@NCNT-800) were synthesized via a facile and economical approach to investigate the efficient degradation of organic pollutants in aqueous environments. This material demonstrated high catalytic efficiency in the degradation of carbamazepine (CBZ) in the presence of peroxymonosulfate (PMS). The experimental data revealed that at a neutral pH of 7 and an initial CBZ concentration of 20 mg/L, the application of Co3@NCNT-800 at 0.2 g/L facilitated a degradation rate of 64.7% within 60 min. Mechanistic investigations indicated that the presence of pyridinic nitrogen and cobalt species enhanced the generation of reactive oxygen species. Radical scavenging assays and electron spin resonance spectroscopy confirmed that radical and nonradical pathways contributed to CBZ degradation, with the nonradical mechanism being predominant. This research presents the development of a novel PMS catalyst, synthesized through an efficient and stable method, which provides a cost-effective solution for the remediation of organic contaminants in water.

Degradation of Water Pollutants by Biochar Combined with Advanced Oxidation: A Systematic Review

Recently, biochar has emerged as a promising option for environmentally friendly remediation due to its cost-effectiveness, extensive surface area, porosity, and exceptional electrical conductivity. Biochar-based advanced oxidation procedures (BC-AOPs) have gained popularity as an effective approach to breaking down organic pollutants in aqueous environments. It is commonly recognized that the main reactive locations within BC-AOPs consist of functional groups found on biochar, which encompass oxygen-containing groups (OCGs), imperfections, and persistent free radicals (PFRs). Additionally, the existence of metallic components supported on biochar and foreign atoms doped into it profoundly impacts the catalytic mechanism. These components not only modify the fundamental qualities of biochar but also serve as reactive sites. Consequently, this paper offers a comprehensive review of the raw materials, preparation techniques, modification approaches, and composite catalyst preparation within the biochar catalytic system. Special attention is given to explaining the modifications in biochar properties and their impacts on catalytic activity. This paper highlights degradation mechanisms, specifically pathways that include radical and non-radical processes. Additionally, it thoroughly examines the importance of active sites as catalysts and the basic catalytic mechanism of BC-AOPs. Finally, the potential and future directions of environmental remediation using biochar catalysts and advanced oxidation processes (AOPs) are discussed. Moreover, suggestions for future advancements in BC-AOPs are provided to facilitate further development.

Development of composite films of bismuthates immobilized in alginate biopolymers for application in photocatalysis under visible light

The immobilization of photocatalysts in films represents an alternative for mitigating the drawbacks associated with suspensions, such as deactivated catalyst separation from the reaction medium. The present study sought to help prevent immobilization from harming the environment through the use of biodegradable alginate films as a matrix. Furthermore, the study employed bismuth-based photocatalysts active in the visible spectrum, making greater use of solar energy. Employing the sol–gel method, the photocatalysts NaBiO3, BiOI, Bi2MoO6, and Bi2WO6 were immobilized to form films, characterized using X-ray diffraction, surface morphology, point of zero charge (pHPZC), and thermogravimetric analysis. The photocatalytic activity of the films was measured by batch assay, using methylene blue and phenol as model molecules. The alginate and NaBiO3 films showed high efficacy for degrading organic pollutants, while BiOI exhibited the highest adsorption rate. The Bi2MoO6 and Bi2WO6 films offered superior stability and efficiency for up to three reuses. The results demonstrated that, by immobilizing photocatalysts in alginate films, photocatalytic activity can be preserved and particle carryover prevented, representing an advancement in sustainable technologies for treating organic pollutants in aqueous environments.

Origins of Selective Oxidation in Carbon-Based Nonradical Oxidation Processes toward Organic Pollutants: Quantitative Structure-Activity Relationships (QSARs).

Metal-free carbon material-mediated nonradical oxidation processes (C-NOPs) have emerged as a research hotspot due to their excellent performance in selectively eliminating organic pollutants in aqueous environments. However, the selective oxidation mechanisms of C-NOPs remain obscure due to the diversity of organic pollutants and nonradical active species. Herein, quantitative structure-activity relationship (QSAR) models were employed to unveil the origins of C-NOP selectivity toward organic pollutants in different oxidant systems. QSAR analysis based on adsorption and oxidation descriptors revealed that C-NOP selectivity depends on the oxidation potentials of organic pollutants rather than on adsorption interactions. However, the dominance of electronic effects in selective oxidation decreases with increasing structural complexity of organic pollutants. Moreover, the oxidation threshold solely depends on the inherent electronic nature of organic pollutants and not on the reactivity of nonradical active species. Notably, the accuracy of substituent descriptors (Hammett constants) and theoretical descriptors (e.g., highest occupied molecular orbital energy, ionization potential, and single-electron oxidation potential) is significantly influenced by the complexity and molecular state of organic pollutants. Overall, the study findings reveal the origins of organic pollutant-oriented selective oxidation and provide insight into the application of descriptors in QSAR analysis.

Effectiveness of Chemical Oxygen Demand as an Indicator of Organic Pollution in Aquatic Environments

The chemical oxygen demand (COD) is an essential indicator of organic pollution that represents the amount of bulk carbon in water. COD is strongly correlated with nutrient cycles and other pollutants in the environment, but it has a limited ability to quantify the amount of organic carbon (OC), of which a large proportion is made up of refractory dissolved organic carbon (RDOC) and is a potential carbon sink. Moreover, the biodegradability of OC in terms of its fate and destination should be explored, as well as how this is reflected by COD. Methods based on particle size, spectroscopy, and isotopic tracing are expected to help with deciphering the bioavailability of COD-responsive OC and explore the processes of biogeochemical cycles. As the pressure on the environment from anthropogenic inputs increases, understanding the bioavailability of OC associated with COD will help with developing more precise scientific indicators for environmental monitoring and identifying how new tools will increase knowledge of the carbon cycle. In this review, we discuss the application, scope, means, and advances of COD measurement. Based on data in the literature, we estimate the global RDOC stock and assess the impact of anthropogenic RDOC on the carbon cycle in offshore bays. This review presents new insights into the behavior of OC in aquatic environments and a potential pathway for ocean negative carbon emissions by expanding the role of RDOC as a carbon sink to offset the effect of anthropogenic carbon emissions.

Catalytic and biological properties of palladium(II) complexes with bidentate Schiff base ligands

In this study, we synthesized and characterized Schiff base ligands (S1–3), which contained sulfonamide/sulfonate groups, and their corresponding Pd(II) complexes (K1–3). We also introduced these complexes into Al2O3‐supported materials (M1–3) using the impregnation method. Following the structural characterization, we proceeded to evaluate the performance of the supported materials in a series of degradation and reduction reactions of involving organic pollutants. These assessments were conducted with the intention of exploring their potential as catalysts in aqueous environments in the presence of NaBH4. The study's findings present novel approaches to develop effective catalysts for reducing/degrading organic pollutants in aqueous environments. The M2 catalyst showed excellent results for dye mixing after 90 s. Additionally, we investigated the antibacterial and cytotoxic properties of the synthesized compounds. The outcome also suggests that these synthesized compounds exhibit potential antibacterial and cytotoxic properties.

Metal-free catalysts with local fluorination regulation for peroxymonosulfate activation: Nearly 100 % singlet oxygen production for selective degradation of aqueous organic pollutants

Generating singlet oxygen (1O2) via activating peroxymonosulfate (PMS) is crucial for the selective removal of organic pollutants in aquatic environments. However, achieving efficient and selective conversion of PMS into 1O2 without consuming energy or metals remains a significant challenge. In this study, graphite phase carbon nitride (g-C3N4) was locally fluorinated via a simple polymerization method. The local fluorinated g-C3N4 (FCN) was used as a metal-free catalyst to activate PMS, enabling highly efficient degradation of 4-chlorophenol (100 %) and detoxification. The FCN/PMS system demonstrates exceptional selectivity for electron-rich pollutants, functions effectively across a broad pH range (2–10), and exhibits remarkable interference resistances to background scavenging ions and natural organic compounds. Furthermore, quenching experiments, probe tests, electron paramagnetic spin resonance measurements, electrochemical characterizations, and theoretical calculations demonstrated that 1O2 was the only reactive species in the catalytic process. Local fluorination regulated the electronic structure of g-C3N4, juxtaposing electron-rich fluorine with electron-deficient carbon dual active sites. This modification alters the electron transfer direction between PMS and g-C3N4, allowing for nearly 100 % selective generation of 1O2via dual electron transfer channels without the need for energy or metals. This study provides a new strategy for designing metal-free heterogeneous catalysts to selectively generate 1O2 in a green way and can facilitate the wider applications of advanced oxidation processes for water purification.

Magnetic perovskite nanohybrid based on g-C3N4 nanosheets for photodegradation of toxic environmental pollutants under short-time visible irradiation

In this study, a magnetic perovskite nanohybrid based on g-C3N4 (gCN) nanosheets was synthesized and developed for the efficient photodegradation of toxic environmental pollutants under short-time visible irradiation. The synthesis of this nanohybrid involved the incorporation of SrTiO3:N (STO:N) and ZnFe2O4 (ZnF) onto the g-C3N4 nanosheets through a simple reflux method. Our investigation encompassed a comprehensive suite of analytical techniques, including BET, TGA, TEM, SEM, EDX, DRS, VSM, XRD, photocurrent, and FT-IR, to elucidate the physicochemical characteristics of this nanocomposite in the context of its application in photodegradation processes. The nanohybrid displayed significantly enhanced photocatalytic activity compared to its individual components, achieving a degradation efficiency of over 90% for various pollutants, including organic dyes like Rhodamine B (Rh-B), within a short irradiation time. This enhanced activity can be attributed to the synergistic effect between gCN, STO:N, and ZnF, which promotes the generation of reactive oxygen species and facilitates the degradation process. Notably, the nanocomposite containing 20 wt% STO:N perovskite and 20 wt% ZnF demonstrated the highest Rh-B degradation rate under visible light irradiation within just 30 min. Furthermore, the nanohybrid displayed excellent stability and reusability over seven consecutive runs, retaining its high photocatalytic activity even after multiple cycles of degradation. This remarkable performance can be attributed to the strong interaction between the gCN nanosheets and the magnetic perovskite components, which prevents their aggregation and ensures their efficient utilization. Additionally, the nanohybrid exhibited excellent visible light absorption, enabling the utilization of a wider range of light for degradation. This feature is particularly advantageous, as visible light is more abundant in sunlight compared to UV light, rendering the nanohybrid suitable for practical applications under natural sunlight. In conclusion, the ternary gCN-STO:N@ZnF nanocomposite represents a promising candidate for the treatment of organic pollutants in aqueous environments, offering a versatile and efficient solution.