Micropollutants In Wastewater Research Articles

Electrochemical UV/Ozone process with Ni-Sb-SnO2/SiOx anode for degradation of micropollutants in wastewater

We investigated the synergistic effects of ozone evolution reaction (OZER) coupled with UV irradiation for degradation of O3-refractory micro-pollutants in electrochemical (E)-UV/O3 process. A SiOx heterojunction layer over-coated on Ni-Sb-SnO2 remarkably enhanced the OZER across a wide pH range (0.4–10). The exceptional OZER efficiency was harnessed in E-UV/O3 to increase degradation rates (by 2.5–3.5-fold) and mineralization efficiencies (by 1.3–3.9-fold) for 2,6-dinitrotoluene (DNT) compared to the sums under dark electrolysis and photolysis. Clarifying DNT degradation intermediates and reactive oxygen species elucidated the promoting mechanism within the reaction network of O3 transformation to ∙OH, the principal oxidant for the supreme performance at near-neutral pH. Applicability of E-UV/O3 was demonstrated by minuscule halate ion generation, outstanding stability and energy efficiency, and elimination of N,N-diethyl-m-toluamide (DEET) in reverse osmosis concentrates (ROC). These comprehensive findings from mechanistic studies to real applications are expected to broaden the utilization of OZER-based water treatments.

Mitigation of caffeine micropollutants in wastewater through Ag-doped ZnO photocatalyst: mechanism and environmental impacts.

Micropollutants, such as caffeine (M-CF), pose a significant threat to ecosystems and human health through water and food sources. The utilization of metal oxide-based photocatalysts has proven to be an effective treatment method for the removal of organic pollutants. This study explores the efficacy of Ag-doped ZnO (Ag/ZnO) for removing M-CF from wastewater. The characterization of Ag/ZnO underscores the crucial role of band gap energy in the photocatalytic degradation process. This parameter influences the separation of electrons and holes (e-/h+) and the generation of reactive radicals. Under solar light, Ag/ZnO demonstrated markedly superior photocatalytic activity, achieving an impressive degradation efficiency of approximately 93.4%, in stark contrast to the 53.2% occurred by ZnO. Moreover, Ag/ZnO exhibited a remarkable degradation efficiency of M-CF in wastewater, reaching 83.5%. A key advantage of Ag/ZnO lies in its potential for recovery and reuse in subsequent treatments, contributing to a reduction in operational costs for industrial wastewater treatment. Impressively, even after five cycles, Ag/ZnO maintained a noteworthy photodegradation rate of M-CF at 78.6%. These results strongly suggest that Ag/ZnO presents a promising solution for the removal of micropollutants in wastewater, with potential scalability for industrial and large-scale applications.

High resolution mass spectrometry-based screening for the comprehensive investigation of organic micropollutants in surface water and wastewater from Pasto city, Colombian Andean highlands

The complexity of the aquatic environment scenario, including the impact of urban wastewater, together with the huge number of potential hazardous compounds that may be present in waters, makes the comprehensive characterization of the samples an analytical challenge, particularly in relation to the presence of organic micropollutants (OMPs). Nowadays, the potential of high-resolution mass spectrometry (HRMS) for wide-scope screening in environmental samples is out of question. Considering the physicochemical characteristics of OMPs, the coupling of liquid (LC) and gas chromatography (GC) to HRMS is mandatory. In this work, we have explored the combined use of LC and GC coupled to Quadrupole-Time-of-Flight Mass Spectrometry (QTOF MS) for screening of surface water and wastewater samples from Pasto (Nariño), a town of the Colombian Andean highlands (average altitude 2527 m), located in an important agricultural area. The upper basin of the Pasto River is impacted by phytosanitary products used in different crops, whereas the domestic wastewater is directly discharged into the river without any treatment, enhancing the anthropogenic impact on the water quality. The OMP searching was made by target (standards available) and suspect (without standards) approaches, using home-made databases containing >2000 compounds. Up to 15 pesticides (7 insecticides, 6 fungicides and 2 herbicides) were identified in the sampling point of the Pasto River up to the town, while no pharmaceuticals were found at this site, illustrating the impact of agriculture practices. On the contrary, 14 pharmaceuticals (7 antibiotics and 3 analgesics, among others) were found in river samples collected in the middle and down to the town sites, revealing the impact of the urban population. Interestingly, some transformation products, including metabolites, such as carbofuran-3-hydroxy and 4-acetylamino antipyrine were identified in the screening. Based on these data, future monitoring will apply target quantitative LC-MS/MS methods for the most relevant compounds identified.

Direct Measurement of Organic Micropollutants in Water and Wastewater Using Fluorescence Spectroscopy

Direct Measurement of Organic Micropollutants in Water and Wastewater Using Fluorescence Spectroscopy

Catchment area, fate, and environmental risks investigation of micropollutants in Danish wastewater

This study aimed to investigate the spatial distribution of micropollutants in wastewater related to catchment area, and their environmental risks and fate. About 24-h flow proportional effluent (n = 26) wastewater samples were collected from eight WWTPs across Denmark. From five of these WWTPs corresponding influent samples (n = 20) were collected. Samples were enriched by multi-layer solid phase and analysed by liquid chromatography–high-resolution mass spectrometry and comprehensive two-dimensional gas chromatography with high-resolution mass spectrometry detection. We detected and quantified 79 micropollutants from a list of 291 micropollutants in at least one influent or effluent wastewater sample. From this we found that 54 micropollutants decreased in concentrations during wastewater treatment, while O-desmethylvenlafaxine, carbamazepine, amitriptyline, benzothiazole, terbutryn, and citalopram increased in concentrations through the WWTP.The toxicity of effluent wastewater samples was assessed by EC50 using Raphidocelis subcapitata (R. subcapitata) and LC50 using the crustacean Daphnia magna (D. Magna), for which six micropollutants were detected above the predicted no-effect concentration. Our study demonstrates that catchment area influences the micropollutant composition of wastewater. Out of 19 pharmaceuticals, the measured concentration in influent wastewater was predicted within a factor of 10 from sale numbers and human excretion, which demonstrates the strong influence of catchment area on micropollutant composition.

A realistic approach to radiation-induced treatment of micropollutants in wastewater

A realistic approach to radiation-induced treatment of micropollutants in wastewater

Potential of Laccase as a Tool for Biodegradation of Wastewater Micropollutants

In the 21st century, humans are facing a high risk of exposure to emerging pollutants. Water contamination has become a major threat due to its devastating impacts on the entire ecosystem. Relatively great danger for aquatic microorganisms is posed by organic micropollutants, which are a consequence of progressing urbanization and industrialization. This review focuses on laccase of mainly fungal and bacterial origin, which provides an eco-friendly strategy for the transformation of these harmful pollutants to less or non-toxic compounds, as it acts oxidatively on the aromatic ring of a wide range of compounds, releasing water as the only by-product. Laccase alone or with the use of mediators has been used successfully to remove micropollutants from wastewater, including pharmaceuticals and personal care products, biocides, endocrine disrupting agents, steroid hormones, and microplastics. Even though the potential of an LMS (laccase–mediator system) is tremendous, the selection of an appropriate mediator and the persistent monitoring of toxicity after treatment are critical and should be performed routinely. Hence, further research is still needed for the optimization of degradation processes to improve our understanding of the different interactions of laccase with the substrate and to develop sustainable advanced water treatment systems.

Promoted micropollutant degradation and structural evolution of natural organic matter by a novel S(IV)-based water treatment strategy

The ubiquity of various organic micropollutants in global water and wastewater has raised considerable concern about their cost-efficient elimination. This study reported that the novel UV365/FeTiOX/S(IV) system could accomplish superior abatement of different micropollutants (e.g., carbamazepine, CMZ) in 30–45 min with excellent reusability and stability of FeTiOX. In addition, this system functioned effectively to remove roxarsone and As(III)/As(V) by catalytic oxidation and adsorption, respectively. Mechanistic investigations suggested the dual roles of S(IV) in enhancing pollutant oxidation, i.e., promoted Fe(II)/Fe(III) cycle and photocatalysis. These processes facilitated the continuous generation of multiple oxidizing intermediates (e.g., hydroxyl radicals, sulfate radicals, and singlet oxygen), in which the last one was first proposed as the main contributor in iron-mediated S(IV)-based oxidation processes. Based on the product identification, the transformation pathways of four different micropollutants were tentatively unraveled. The in silico prediction suggested the lower environmental risks of the final reaction products than the precursors. Particularly, the structural alteration of humic acid was analyzed, indicating an increased O/C ratio after oxidative treatment. Overall, this study has implications for developing an efficient oxidation technique for removing multiple micropollutants in water and facilitating the mechanistic reactivity modulation of the S(IV)-based oxidation strategies in water treatment.

Degradation of methotrexate by unactivated and solar-activated peroxymonosulfate in water: Moiety-specific reaction kinetics and transformation product-associated risks

Anticancer drugs have raised worldwide concern owing to their ubiquitous occurrence and ecological risks, necessitating the development of efficient removal strategies in water and wastewater treatment. Although peroxymonosulfate (PMS) is known to be a promising chemical in water decontamination, limited information is available regarding the removal efficiency of anticancer drugs by PMS and solar/PMS systems. This study first reports the moiety-specific reaction kinetics and mechanisms of methotrexate (MTX), an anticancer drug with widespread attention, by PMS (unactivated) and solar-activated PMS in water. It was found that MTX abatement by the direct PMS oxidation followed second-order kinetics, and the pH-dependent rate constants increased from 0.4 M−1 s−1 (pH 5.0) to 1.3 M−1 s−1 (pH 8.0), with a slight decrease to 1.1 M−1 s−1 at pH 9.0. The presence of chloride and bromide exerted no obvious influence on the removal of MTX by PMS. Furthermore, the chemical reactivity of MTX and its seven substructures with different reactive species was evaluated, and the degradation contributions of the reactive species involved were quantitatively analyzed in the solar/PMS system. The product analysis suggested similar reaction pathways of MTX by PMS and solar/PMS systems. The persistence, bioaccumulation, and toxicity of the transformation products were investigated, indicating treatment-driven risks. Notably, MTX can be removed efficiently from both municipal and hospital wastewater effluents by the solar/PMS system, suggesting its great potential in wastewater treatment applications. Overall, this study systematically evaluated the elimination of MTX by the unactivated PMS and solar/PMS treatment processes in water. The obtained findings may have implications for the mechanistic understanding and development of PMS-based processes for the degradation of such micropollutants in wastewater.

Solvothermal synthesis of 3D rod-shaped Ti/Al/Cr nano-oxide for photodegradation of wastewater micropollutants under sunlight: a green way to achieve SDG:6.

Waterbodies are day-by-day polluted by the various colored micropollutants, e.g., azo dyes enriched (carcinogenic, non-biodegradable) colored wastewater from textile industries. Water pollution has become a serious global issue as ~ 25% of health diseases are prompted by pollution as reported by WHO. Around 1 billion people will face water scarcity by 2025 and this water crisis is also a prime focus to the UNs' sustainable development goal 6 (SDG6: clean water and sanitation). To prevent the water pollution caused by micropollutants, a mesoporous, 3D rod-like nano-oxide Ti/Al/Cr (abbreviated as TAC) has been synthesized via the solvothermal method. TAC degraded all classes of azo dyes (mono, di, tri, etc.) with > 90% efficiency under renewable energy source solar irradiation within the pH range 2-11. The detailed study was done on the photodegradation of carcinogenic di-azo dye Congo red (CR) which is banned in many countries. TAC showed 90.64 ± 2% degradation efficiency for CR at pH 7. The proposed photodegradation mechanism of CR was confirmed by the high-resolution liquid chromatography-mass spectroscopy (HRLC-MS) analysis obeying the Pirkanniemi path. The photodegradation obeyed the pseudo-1st-order kinetics and was reusable up to successive 5 cycles which can be an efficient tool to meet the UNs' SDG:6.

Packed OV-SnO2-Sb bead-electrodes for enhanced electrocatalytic oxidation of micropollutants in water

Electrocatalytic oxidation is an appealing treatment option for emerging micropollutants in wastewater, however, the limited reactive surface area and short service lifetime of planar electrodes hinder their industrial applications. This study introduces an innovative electrochemical wastewater treatment technology that employs packed bead-electrodes (PBE) as a dynamic electrocatalytic filter on a dimensionally stable anode (DSA) acting as a current collector. By using PBE, the electroactive volume is expanded beyond the vicinity of the common planar anode to the thick porous media of PBE with a vast electrocatalytic surface area. This greatly enhances the efficiency of electrochemical degradation of micropollutants. The OV-SnO2-Sb PBE filter achieved a nearly 100 % degradation of moxifloxacin (MOX) in under 2 min of single-pass filtration, with a degradation rate over an order of magnitude higher than the conventional electrochemical oxidation processes. The generation of abundant radical species (•OH) and non-radical species (1O2 and O3), along with the enhanced direct oxidation, led to the outstanding performance of the charged PBE system in MOX degradation. The OV-SnO2-Sb PBE was remarkably stable, and the separation between the electroactive PBE layer and the base Ti anode allows for easy renewal of the bead-electrode materials and scaling up of the system for practical applications. Overall, our study presents a dynamic electroactive PBE that advances the electrocatalytic oxidation technology for effective control of emerging pollutants in the water environment. This technology has the potential to revolutionize electrochemical wastewater treatment and contribute to a more sustainable future environment.

Micropollutant concentration fluctuations in combined sewer overflows require short sampling intervals

Combined sewer overflows (CSOs) are an important pathway of organic micropollutants from urban areas to open water bodies. Understanding the temporal dynamics of these micropollutants during overflow events is crucial for applying appropriate sampling methods and implementing effective management strategies. Yet, little is known about the dynamics of micropollutants in CSOs, because most studies report concentrations from single grab samples or event mean concentrations (EMCs). With unique high temporal resolution measurements (3 min), we show the real dynamics of polar organic micropollutants in CSOs of one small (2,700 people: P) and one large (159,000 P) urban catchment, for two micropollutant categories: (i) 33 micropollutants in municipal wastewater and (ii) 13 micropollutants from urban surface runoff. The concentration dynamics depend on the substance source and the catchment size. Indoor substances such as pharmaceuticals show high temporal dynamics with changes of 1 to 2 orders of magnitude within 9 min in the CSO of the small catchment. In contrast, outdoor substances at the small catchment and all substances at the large catchment display considerably lower variation. We tested various time-proportional sampling strategies to assess the range of error when estimating EMCs. We recommend an interval of 3 min to capture the dynamics of indoor substances in CSOs from small catchments. The results highlight that both future monitoring campaigns and the planning and management of urban wet-weather treatment systems will benefit from high temporal sampling resolutions, not only to understand dynamics but also to minimize errors of estimated EMCs.

Porous cyclopentadiene unit-incorporated graphitic carbon nitride nanosheets for efficient photocatalytic oxidation of recalcitrant organic micropollutants in wastewater

For the purpose of searching for efficient photocatalysts to deal with recalcitrant organic micropollutants in wastewater, here an in-situ supramolecule self-assembly-thermal polymerization strategy is developed to prepare a series of porous cyclopentadiene (CPD) unit-incorporated g-C3N4 ultrathin nanosheets (CCPD-g-C3N4). The CCPD-g-C3N4 demonstrate CPD unit doping level-dependent and remarkably enhanced visible-light photocatalytic oxidation efficiency towards two organic micropollutants, acetaminophen and methylparaben, in which the optimized CCPD-g-C3N4-2 shows 6.1 and 3.5 times higher acetaminophen and methylparaben degradation rate than bulk g-C3N4; moreover, CCPD-g-C3N4-2 is still robust and efficient in the treatment of five mixed organic micropollutants in pharmaceutical wastewater, and the satisfactory micropollutant removal efficiency is obtained in a wide pH window and the presence of high concentrations of inorganic anions and cations as well as dissolved organic matters. Theoretical calculation combined with experimental test reveal that CCPD-g-C3N4 can significantly reduce ecological risk of the target pollutant after the photocatalytic degradation reaction. Such enhanced photocatalytic oxidation efficiency is dominated by the accelerated charge carrier separation dynamics and extended visible-light response region due to the incorporation of CPD units, which finally lead to the generation of abundant reactive oxygen species to degrade and mineralize target micropollutants efficiently.

Fate of micropollutants in a lab-scale urban wastewater system: Impact of iron-rich drinking water treatment sludge

Iron rich drinking water treatment sludge (Fe-DWTS) could be a potential alternative for Fe salts in controlling sulfide in the sewer network. This study investigated the impact of in-sewer dosed Fe-DWTS on the fate of 26 different intrinsic organic micropollutants in wastewater by using a lab-scale integrated system consisting of sewer reactors and a sequential batch reactor (SBR) to simulate urban wastewater collection and treatment. The batch results revealed that seven among these 26 compounds had higher removal in the Fe-DWTS dosed sewer reactor compared to the control sewer reactor. In contrast, the removal of 7 out of the 26 investigated compounds were reduced, along with the biofilm methanogenic activity due to the long-term Fe-DWTS dosing. Cycle experiments in the SBR showed that the removal of acesulfame was enhanced and the formation of carbamazepine, desvenlafaxine, tramadol and hydrochlorothiazide were reduced, compared to their behaviour in the control SBR. However, the long-term experiments showed no adverse or beneficial effect of in-sewer dosed Fe-DWTS on the removal of most micropollutants in the SBR. Codeine, trimethoprim and gabapentin were exceptions with slightly higher concentrations in the experimental SBR effluent, possibly due to change in microbial composition.

A sustainable system for decontamination of cephalexin antibiotic using electrocoagulation technology and response surface methodology

AbstractThe emergence of synthetic micropollutants in wastewater due to domestic and industrial use has presented new challenges for treatment processes. Among these pollutants, pharmaceutical and personal care products (PPCPs) are considered emerging contaminants due to their potential to enter drinking water sources. Antibiotics, in particular, are of significant concern due to their high consumption in veterinary and human applications. In this study, the electrocoagulation (EC) process is used as an efficient technique for the removal of cephalexin (CFX) from pharmaceutical wastewater. The study aims to explore the ability of the EC process to remove CFX and optimize its performance using the response surface method based on Central Composite Design (RSM‐CCD). The effects of initial CFX concentration, electrolysis time, initial pH, and electrode type (non‐insulated and insulated) were considered in the optimization process. This research is distinct as it examines the influence of key factors on the elimination of CFX. The results showed that electrolysis time had the most significant effect on CFX removal using the EC process. The analysis of variance (ANOVA) test was used to evaluate the importance of independent variables and their interaction. The optimal operating conditions for maximum removal efficiency (86.53%) were an initial CFX concentration, reaction time, and initial pH of 34 mg/L, 34.35 min, and 6.5, respectively, using an insulated electrode. Under these optimal conditions, predicted CFX removal was 93.54%. These findings demonstrate that RSM‐CCD is a useful tool for optimizing electrochemical removal processes for micropollutants such as CFX from wastewater streams. The study highlights the importance of considering electrode type in optimizing EC processes for micropollutant removal from wastewater.

Removal of Ibuprofen and Diclofenac in Batch Nitrifying Reactors: Effect of Natural Zeolite on the Process

Ibuprofen (IBP) and diclofenac (DFC) are two of the most commonly used non-steroidal anti-inflammatory drugs (NSAIDs) to treat inflammation and pain. However, they can impact the environment if not treated adequately before discharge into waterways. Biodegradation through the nitrification process is an alternative to reducing the concentration of these micropollutants (MPs) in wastewater. Thus, this work aimed to evaluate the effect of natural zeolite on IBP and DFC removal in a nitrifying batch reactor. Mini-reactors were set up with 90 mL of inoculum and 110 mL of synthetic wastewater with a concentration of 25 mg total ammonia nitrogen TAN/L, at 25 °C and 1 vvm (volume of air/volume liquid∙min) of aeration. Two conditions were tested: high concentrations (IBP = 700 μg/L, DFC = 100 μg/L) and low concentrations (IBP = 30 μg/L, DFC = 20 μg/L). The research used a concentration of 5 g/L of the natural zeolite. Results indicated that the zeolite negatively affected the nitrification rate. At high MPs concentration, the natural zeolite negatively affects the removal of IBP and DFC, where biodegradation and sorption are the mechanisms that eliminate both NSAIDs. Conversely, at low DFC and IBP concentrations, the natural zeolite improves the removal of IBP and DFC, wherein biodegradation is the primary removal mechanism.

Semirigid Highly Conjugated Zirconium-Organic Framework for the Capture of Micropollutants and Solar-Light Photodegradation.

Micro-organic pollutants, particularly organic dyes and personal care products (PPCPs), are widely present in wastewater, and thus pose a serious risk to human health. The capture and solar-light photodegradation of micro-organic pollutants are highly challenging tasks, which require the design and synthesis of microporous materials with specific structures. As we know, organic dyes and PPCPs can be absorbed via π-π* stacking. In this paper, an iron-based metal-organic framework (Fe-UiO-68-terNap) containing semirigid conjugated aromatic ligands is prepared for the capture and solar-light photodegradation of multiple water contaminants. UiO-68-terNap was synthesized based on ternaphthalene with π-π* stacking, which would increase the adsorption capacities of organic micropollutants in wastewater. Additionally, the formation of Fe-O-Zr enhances the charge-separation ability resulting in the successful degradation of micropollutants in 240 min. The novel material has been elucidated by single-crystal X-ray diffraction and Fe K-edge XANES, which provide key insights at a molecular level for the design of novel materials for the capture and photodegradation of organic micropollutants.

Picolinic Acid-Mediated Catalysis of Mn(II) for Peracetic Acid Oxidation Processes: Formation of High-Valent Mn Species.

Metal-based advanced oxidation processes (AOPs) with peracetic acid (PAA) have been extensively studied to degrade micropollutants (MPs) in wastewater. Mn(II) is a commonly used homogeneous metal catalyst for oxidant activation, but it performs poorly with PAA. This study identifies that the biodegradable chelating ligand picolinic acid (PICA) can significantly mediate Mn(II) activation of PAA for accelerated MP degradation. Results show that, while Mn(II) alone has minimal reactivity toward PAA, the presence of PICA accelerates PAA loss by Mn(II). The PAA-Mn(II)-PICA system removes various MPs (methylene blue, bisphenol A, naproxen, sulfamethoxazole, carbamazepine, and trimethoprim) rapidly at neutral pH, achieving >60% removal within 10 min in clean and wastewater matrices. Coexistent H2O2 and acetic acid in PAA play a negligible role in rapid MP degradation. In-depth evaluation with scavengers and probe compounds (tert-butyl alcohol, methanol, methyl phenyl sulfoxide, and methyl phenyl sulfone) suggested that high-valent Mn species (Mn(V)) is a likely main reactive species leading to rapid MP degradation, whereas soluble Mn(III)-PICA and radicals (CH3C(O)O• and CH3C(O)OO•) are minor reactive species. This study broadens the mechanistic understanding of metal-based AOPs using PAA in combination with chelating agents and indicates the PAA-Mn(II)-PICA system as a novel AOP for wastewater treatment.

Selective Transformation of Micropollutants in Saline Wastewater by Peracetic Acid: The Overlooked Brominating Agents.

Peracetic acid (PAA) is an emerging alternative disinfectant for saline waters; HOBr or HOCl is known as the sole species contributing to halogenation reactions during PAA oxidation and disinfection. However, new results herein strongly indicated that the brominating agents (e.g., BrCl, Br2, BrOCl, and Br2O) are generated at concentrations typically lower than HOCl and HOBr but played significant roles in micropollutants transformation. The presence of Cl- and Br- at environmentally relevant levels could greatly accelerate the micropollutants (e.g., 17α-ethinylestraiol (EE2)) transformation by PAA. The kinetic model and quantum chemical calculations collectively indicated that the reactivities of bromine species toward EE2 follow the order of BrCl > Br2 > BrOCl > Br2O > HOBr. In saline waters with elevated Cl- and Br- levels, these overlooked brominating agents influence bromination rates of more nucleophilic constituents of natural organic matter and increase the total organic bromine. Overall, this work refines our knowledge regarding the species-specific reactivity of brominating agents and highlights the critical roles of these agents in micropollutant abatement and disinfection byproduct formation during PAA oxidation and disinfection.

Preparation and visible light catalytic degradation of magnetically recyclable ZnFe2O4/BiOBr flower-like microspheres

The construction of a binary heterojunction is a crucial method for solving the low separation efficiency and photon utilization of BiOBr (BOB) photogeneration carriers. In this study, magnetic recyclable ZnFe2O4/BiOBr (ZFB) heterojunction microspheres containing oxygen vacancies were prepared using a two-step solvothermal method. The results of X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, and Brunauer–Emmett–Teller analysis show that ZnFe2O4 (ZFO) induces the growth of a nanolayer structure on the surface of BOB, the diffraction peak intensity ratio of I(102)/I(110) increases, and the specific surface area increases significantly. The analysis of photoelectric characteristics indicates that compared with BOB, ZFB has a smaller bandgap, a larger visible response range, and a higher photogenerated carrier migration and separation efficiency. ZFB can significantly degrade the activated benzene ring in organic molecules, with the degradation efficiency of Rhodamine B (RhB), norfloxacin (NOR), and sulfadiazine (SDZ) reaching 99.04 %, 91.70 %, and 86.64 %, respectively. Under the magnetic recovery, the five-cycle degradation performance retention rate reaches more than 92 %. Holes and superoxide radicals are the main active substances of ZFB photocatalytic materials for degradation of micropollutants. This research provides an idea for the preparation of a green and efficient photocatalytic material with high recyclable efficiency, which can simultaneously degrade various micropollutants in organic wastewater.