Organic Pollutants In Aquatic Environment Research Articles

2D/2D Heterojunction of BiOBr/BiOI Nanosheets for In Situ H2 O2 Production and Activation toward Efficient Photocatalytic Wastewater Treatment.

The presence of toxic organic pollutants in aquatic environments poses significant threats to human health and global ecosystems. Photocatalysis that enables in situ production and activation of H2 O2 presents a promising approach for pollutant removal; however, the processes of H2 O2 production and activation potentially compete for active sites and charge carriers on the photocatalyst surface, leading to limited catalytic performance. Herein, a hierarchical 2D/2D heterojunction nanosphere composed of ultrathin BiOBr and BiOI nanosheets (BiOBr/BiOI) is developed by a one-pot microwave-assisted synthesis to achieve in situ H2 O2 production and activation for efficient photocatalytic wastewater treatment. Various experimental and characterization results reveal that the BiOBr/BiOI heterojunction facilitates efficient electron transfer from BiOBr to BiOI, enabling the one-step two-electron O2 reduction for H2 O2 production. Moreover, the ultrathin BiOI provides abundant active sites for H2 O2 adsorption, promoting in situ H2 O2 activation for •O2 - generation. As a result, the BiOBr/BiOI hybrid exhibits excellent activity for pollutant degradation with an apparent rate constant of 0.141 min-1 , which is 3.8 and 47.3 times that of pristine BiOBr and BiOI, respectively. This work expands the range of the materials suitable for in situ H2 O2 production and activation, paving the way toward sustainable environmental remediation using solar energy.

Simultaneous adsorption and biodegradation of oxytetracycline in wastewater by Mycolicibacterium sp. immobilized on magnetic biochar

Due to the adverse effects of long-term oxytetracycline (OTC) residues in aquatic environments, an effective treatment is urgently needed. Immobilized microbial technology has been widely explored in the treatment of various organic pollutants in aquatic environments with its excellent environmental adaptability. Nevertheless, studies on its application in the removal of antibiotics are relatively scarce and not in sufficient depth. Only a few studies have further investigated the final fate of antibiotics in the immobilized bacteria system. In this study, a novel kind of OTC-degrading bacteria Mycolicibacterium sp. was immobilized on straw biochar and magnetic biochar, respectively. Magnetic biochar was proved to be a more satisfactory immobilization carrier due to its superior property and the advantage of easy recycling. Compared with free bacteria, immobilized bacteria had stronger environmental adaptability under different OTC concentrations, pH, and heavy metal ions. After 5 cycles, immobilized bacteria could still remove 71.8% of OTC, indicating that it had a stable recyclability. Besides, OTC in real swine wastewater was completely removed by immobilized bacteria within 2 days. The results of FTIR showed that bacteria were successfully immobilized on biochar and O–H, N–H, and C–N groups might be involved in the removal of OTC. The fate analysis indicated that OTC was removed by simultaneous adsorption and biodegradation, while biodegradation (92.8%) played a dominant role in the immobilized bacteria system. Meanwhile, the amount of adsorbed OTC (7.20%) was rather small, which could effectively decrease the secondary pollution of OTC. At last, new degradation pathways of OTC were proposed. This study provides an eco-friendly and effective approach to remedy OTC pollution in wastewater.

Unraveling the single-atom Fe–N4 catalytic site selectivity generate singlet oxygen via activation of persulfate: Polarizing electric fields changes the electron transfer pathway

Single-atom catalysts have been proved to be an effective material for the removal of organic pollutants from water and wastewater, and yet, the relationship between their internal structures and their roles still remains elusive. In this work, a catalyst Fe (MIL)-SAC with single-atom Fe–N4 active site was prepared. Fe (MIL)-SAC/Peroxydisulfate (PDS) system was able to achieve complete degrade of the Sulfamethoxazole (SMX) with kobs at 0.466 min−1, which was faster than the Fenton system under the same conditions (kobs = 0.422 min−1) and 16 times faster than Fe (MIL) (kobs = 0.029 min−1). Density functional calculations reveal that the Fe–N4 structure will affect the electron transport path and lead to selective generation of 1O2 by triggering S–O breakage and O–O polarization in PDS. Furthermore, Fe (MIL)-SAC/PDS system exhibits strong resistance to common influencing factors and has good application prospects. This work provides a new approach for the selectively generation of 1O2 for the efficient treatment of organic pollutants in aqueous environment.

Insights into Photo/Electrocatalysts for the Degradation of Per- and Polyfluoroalkyl Substances (PFAS) by Advanced Oxidation Processes

Per- and polyfluoroalkyl substances (PFASs) are an emerging group of persistent organic pollutants in aquatic environments with high levels of toxicity and bioaccumulation. The risks posed by PFASs to the environment and health have attracted increasing attention. To remove them from water, advanced oxidation processes (AOPs), with the merits of high efficiency and low cost, are mainly used. Photo/electrocatalytic heterogeneous AOPs, with the assistance of nanostructured catalysts and external energy in the form of light/electricity, have emerged as one of the most powerful techniques, overcoming the difficulty associated with defluorination and achieving the effective and complete degradation of PFASs in water. The structures of photo/electrocatalysts play a critical role in the production of reactive oxygen species, the electron transfer process, and the degradation pathway and its efficiency. Herein, to elucidate the structure–performance relationship, a review of photo/electrocatalysts for the enhanced degradation of PFASs in heterogeneous AOPs, organized according to their composition and nanostructure design, is provided. This review article is mainly focused on (1) the mechanisms and pathways of PFAS degradation by heterogeneous photo/electrocatalytic AOPs, and (2) the structural designs and modifications of photo/electrocatalysts for the enhanced degradation of PFASs by heterogeneous AOPs. Finally, the challenges and prospects for future research into photo/electrocatalysts of heterogeneous AOPs in the field of PFAS remediation are discussed.

Enhanced removal efficiency of bensulfuron-methyl by a novel boron doping biochar-based Acinetobacter YH0317 at a lower temperature

Biochar-based bacteria are regarded as an efficient strategy for remediating organic pollutants in aquatic environments. Herein, a strain named Acinetobacter YH0317 that could degrade bensulfuron-methyl (BSM) at a lower temperature (15 °C) was isolated from a paddy rice field with long-term BSM application. Then Acinetobacter YH0317 was loaded on unmodified biochar (BC) and boron doping biochar (BBC). Results showed that BBC-based YH0317 significantly enhanced the removal efficiency of BSM (71.8–99.1%) compared with BC-based YH0317 (41.9–44.0%) and YH0317 alone (18.1–20.7%) in 24 h. BBC promoted the growth of YH0317 and secretion of extracellular secretions by providing a carrier and shelter for YH0317. The electrochemical analysis suggested BBC improved the electron transfer rate, which ultimately facilitated the removal of BSM. Hydroponic experiments indicated that BBC-based YH0317 effectively improved the growth of soybean. This work reports a novel BBC-based Acinetobacter YH0317 that could effectively remediate BSM contamination in the water environment.

Photocatalytic Degradation of Ciprofloxacin with Supramolecular Materials Consisting of Nitrogenous Organic Cations and Metal Salts

The design and synthesis of composite materials with new structures/properties have important practical significance for the degradation of organic pollutants in aquatic environments. On this basis, five new supramolecular materials {[L1]2·[Cu4I8]}(1), {[L1]2·[Ag4I8]}(2), {[L2]·[ZnBr4]}(3), {[L3]2·[AgI5]}(4), {[L3]·[CdBr3Cl]}(5) were synthesized by introducing an amino group into a series of nitrogen-containing cationic ligands (L1–L3) through the reaction of polybromomethylbenzene with 4-aminopyridine. The degradation effect of catalysts 1–5 on ciprofloxacin (CIP) under visible light was studied using their potential catalytic properties. The results showed that compounds 1 and 4 had better degradation effects compared to other compounds. Moreover, compounds 1 and 4 were proved to be excellent catalysts for the photocatalytic degradation of CIP with cyclic experiments. Through further exploration, it was found that neutral conditions and 20 mg compound dosage were more conducive to the photodegradation of CIP by the compound. Through free radical capture experiments, it was found that ·OH played a major role in the photodegradation of CIP.

Anionic and cationic dyes removal by degradation via photoelectrocatalysis using a WO3/CuWO4 heterojunction film as a photoanode

Population growth increases the disposal of organic pollutants in aqueous environments, including anionic and cationic dyes. Tungsten trioxide (WO3) and copper tungstate (CuWO4) have been considered as photocatalysts for the degradation of these pollutants by photoelectrocatalysis. However, these semiconductors used individually have some properties that reduce their potential for application in photoelectrocatalysis. Thus, this work proposed the in-situ synthesis of a WO3/CuWO4 heterojunction film for photoelectrocatalysis of anionic and cationic dyes. The structural characterization showed the monoclinic and triclinic phases in the nanocomposite corresponding to WO3 and CuWO4, respectively. The optical characterization revealed a better visible light absorption for the heterojunction film. The film formed nanoplates grown perpendicular on the conductive substrate, which can mitigate the charge recombination process. The photoelectrochemical characterizations showed superior photoelectrochemical stability for the WO3/CuWO4 film and the best activity to remove cationic dyes.

Cobalt-loaded carbon nanotubes boosted aerobic ciprofloxacin transformation driven by sulfide: A comprehensive mechanism investigation

Sulfide oxidation under aerobic conditions can produce active oxygen for the transformation of organic pollutants in aquatic environments. However, the catalytic performance of transition metal-supported carbon material on this process is poor understood. This study found that Co-loaded carbon nanotubes (CNTs) was able to realize the efficient aerobic transformation of antibiotic ciprofloxacin (CIP) by sulfide, with the pseudo-first order reaction rate constant improved from 0.013 h−1 without catalyst to 0.44–0.71 h−1 with 100 mg/L Co-loaded CNTs. Singlet oxygen (1O2) was the main active specie playing key roles in the process of CIP aerobic transformation with presence of Co-loaded CNTs. Mechanism studies indicated that the excellent electron transfer ability of Co-loaded CNTs might play an important role to promote the electron transfer and facilitate the formation of intermediate H2O2 and 1O2. Additionally, the Co-loaded CNTs/sulfide system effectively reduced the acute toxicity of organic pollutant, and Co-loaded CNTs showed remarkable cycling stability and negligible leaching. This study gives a better understanding for the Co-loaded CNTs mediated aerobic antibiotics transformation by sulfide, and provide a reference for the application of Co-loaded carbon materials on organics aerobic transformation by sulfide.

Recognition, possible source, and risk assessment of organic pollutants in surface water from the Yongding River Basin by non-target and target screening

Organic pollutants in aquatic environment could have important implications on pollution stress on aquatic organisms and even on the risk of human exposure. Thus, revealing their occurrence in aquatic environment is essential for water quality monitoring and ecological risk purposes. In this study, a comprehensive two-dimensional gas chromatography connected with time-of-flight mass spectrometry (GC × GC-TOF-MS) was applied, to enable non-target and target analysis of pollutants in the Yongding River Basin. Based on the isotopic patterns, accurate masses and standard substances, certain environmental contaminants were tentatively identified which including polycyclic aromatic hydrocarbon (PAHs), organochlorine pesticides (OCPs), phenols, amines, etc. The compounds with the highest concentration were naphthalene (109.0 ng/L), 2,3-benzofuran (51.5 ng/L) and 1,4-dichlorobenzene (35.9 ng/L) in Guishui River. Wastewater treatment plants (WWTPs) discharges were a main source of pollutants in Yongding River Basin, as the types of compounds screened in the downstream river were relatively similar to those from WWTPs. According to the target analysis, a number of pollutants were selected due to the acute toxicity and cumulative discharge from WWTPs and downstream rivers. Three PAHs (naphthalene, Benzo(b)fluoranthene and pyrene) homologues showed moderate risk to fish and H. Azteca in Yongding River Basin, while the rest of the measured chemicals showed low ecological impact across the entire study area based on the risk assessment. The results are helpful for understanding the necessity of high-throughput screening analysis for assessing water quality of rivers and the discharge emissions of pollutants from WWTPs to the river environment.

Algae-derived metal-free boron-doped biochar acts as a catalyst for the activation of peroxymonosulfate toward the degradation of diclofenac

In this study, plain seaweed biochar (SW) and boron-doped seaweed biochar (BSW) were prepared through a simple pyrolysis process using Undaria pinnatifida (algae biomass) and boric acid. The BSW catalyst was utilized to degrade organic pollutants in aqueous environments by activating peroxymonosulfate (PMS). Surface characterization of the BSW demonstrated successful doping of boron into the biochar materials. BSW600 exhibited greater catalytic activity than SW600, as evidenced by the former's maximum adsorption capacity of diclofenac (DCF) onto BSW600 (qmax = 30.01 mg g−1) and the activation of PMS. Complete degradation of DCF was achieved in 30 min using 100 mg L−1 BSW600, 0.5 mM PMS, and 6.5 initial solution pH as critical parameters. The pseudo-first-order kinetic model accurately described the DCF degradation kinetics. The scavenger experiment displayed that radical and non-radical reactive oxygen species (ROS) formed in the BSW600/PMS system. Furthermore, the generation of ROS in the BSW600/PMS system was confirmed by electron spin resonance spectroscopy (ESR). The percentage contribution of ROS was assessed to be 12.3, 45.0, and 42.7% for HO•, SO4•–, and 1O2, respectively. Additionally, the electron transfer pathway was also confirmed by electrochemical analysis. Moreover, the influence of water matrics on the BSW600/PMS system was demonstrated. The co-existence of anions and humic acid (HA) did not affect the catalytic activity of the BSW600/PMS system. The recyclability of BSW600 was assessed by DCF removal (86.3%) after three cycles. Ecological structure-activity relationships software was used to assess by-product toxicity. This study demonstrates the efficacy of non-metallic heteroatom-doped biochar materials as eco-friendly catalysts in groundwater applications.

Studying the destruction of pollutant in the presence of photocatalysts based on MWCNTs with controlled values of TiO2 nanoparticles

The main goal of the present research is the synthesis of new photocatalysts to reduce the amount of organic pollutants in aquatic environments. For this purpose, the amount of TiO2 nanoparticles in the synthesized samples containing MWCNTs is controlled to synthesize two types of photocatalysts named as MCT#1 and MCT#2. Samples characterizing using XRD reveal that the TiO2 nanoparticles have a combined phase of rutile and anatase. So that in both of photocatalysts, the percentage of anatase phase is higher than rutile. The analysis of the degradation rate demonstrates that intensification level of TiO2 nanoparticles in MCT#2 compared to the MCT#1 leads to enhancement of photocatalytic activity of MCT#2. Design of experiment results shows that the destruction amount of MO is affected by irradiation time and pH. Based on ANOVA study, it is observed that both factors have a significant effect on reducing of MO concentration. Analyzing the results based on Duncan's multiple range test at α = 0.05 confirm that all the studied levels of the main parameters have a logical influence on MO destruction. Meanwhile, it can be deducted that the most and the least of destruction is observed at pH = 7 and pH = 3, respectively.

Preparation of magnetic Fe3O4@PDA/CuS core-shell nanocomposite as a green photocatalyst

To solve the emerging aromatic organic pollutants in aqueous environment, in this study, the efficient recyclable core-shell structured photocatalyst Fe3O4@PDA/CuS was prepared by in situ reduction method. Firstly, Fe3O4 as cores were prepared to provide magnetic recovery. Through the self-polymerization of dopamine (DA), polydopamine (PDA) was coated on Fe3O4 as shells to protect Fe3O4 cores. Then, Cu2+ coordinated with PDA on the surface of Fe3O4@PDA and in situ reduced by Na2S to obtain core-shell structural Fe3O4@PDA/CuS with CuS uniformly growing on the PDA. CuS with a narrow band gap will endow Fe3O4 @PDA/CuS excellent photocatalytic performance for organic dyes degradation. The decomposition rate of methylene blue (MB) reached to 92.1 % within 180 min under visible light irradiation of Fe3O4@PDA/CuS as photocatalyst without any cocatalyst. When pH= 10, the decomposition rate of MB can reach to 92.7 % in 60 min, indicated Fe3O4@PDA/CuS was more suitable for use under alkaline conditions. The capture experiment determined that·OH was the main active substance. This also explained that under alkaline conditions, numerous OH- was conducive to the formation of ·OH, thus accelerated the degradation rate. And the decomposition rate of MB by Fe3O4@PDA/CuS can still reach 83.95 % after reused three times.

N and S co-doped pine needle biochar activated peroxydisulfate for antibiotic degradation

A low-cost nitrogen and sulfur doped biochar (CNS) was prepared by oxygen limiting method using pine needles. In the CNS/PDS system, the degradation rate of tetracycline hydrochloride (TCH) reached 85.6% in 20 min when the pyrolysis temperature was 800 °C. X-ray photoelectron spectroscopy and Raman spectroscopy showed that high-temperature pyrolysis produced more carbonyl and defect, which enhanced the activation efficacy of CNS for PDS. Electron paramagnetic resonance and radical quenching have demonstrated that O2•- and 1O2 played key roles in radical pathway. A novel mechanism for degradation of TCH by electron transfer pathway was proposed by linear sweep voltammetry and electrochemical impedance spectroscopy. CNS served as a transport mediator and the electrons of TCH were continuous transferred to PDS via CNS, which accelerated its oxidation. Moreover, density functional theory demonstrated that pyrrolic N combined with the H atom of PDS to form an N–H structure and generated a PDS-catalyst complex. The projected density of state results showed that pyrrolic N and thiophene S further speeded up the electron transfer process due to their closer proximity to 0 Fermi level. This study provides insight into the reaction mechanism of heteroatom doped biochar for treatment of organic pollutants in aquatic environments.

Zero-Valent Copper-Mediated Peroxymonosulfate Activation for Efficient Degradation of Azo Dye Orange G

Zero-valent metal (ZVMs)-based persulfate activation systems are extensively applied for the elimination of organic pollutants in aqueous environments. In this study, for the first time, zero-valent copper (ZVC) was employed as the peroxymonosulfate (PMS) activator for the efficient degradation of Orange G (OG). The physicochemical properties of ZVC were systematically characterized by FESEM, EDX, TEM, XRD and XPS measurements. Furthermore, the effects of catalyst loading, PMS dosage, OG concentration and inorganic anions on the ZVC/PMS system were, respectively, investigated and explicated. The formation of •OH and SO4•− in the system was verified by quenching experiments and then the possible reaction mechanism was proposed. This work can provide insight into water treatment technology based on ZVMs.

Comparison of modes of action between fish, cell and mitochondrial toxicity based on toxicity correlation, excess toxicity and QSAR for class-based compounds

Mitochondria are significant targets in cells for many environmental chemicals. Mitochondrial damage and dysfunction can lead to apoptosis and death of fish. The objectives of this study were to compare the modes of action (MOAs) between fish, cell and mitochondrial toxicity. To achieve the goal, toxicity correlation, excess toxicity and quantitative structure–activity relationship (QSAR) were investigated between these three toxicity endpoints for a wide range of compounds. Results showed that fish toxicity is well correlated to cytotoxicity, but overall fish toxicity is relatively greater than the cytotoxicity. On the other hand, fish or cell toxicity is poorly related to mitochondrial toxicity, suggesting some compounds share same toxic mechanism but some not. The excess toxicity calculated from toxicity ratio (TR) shows that specifically-acting compounds in cytotoxicity, such as insecticides, fungicides, herbicides, dyes and medications used to treat cancer, depression, heart failure and blood pressure, are active compounds in mitochondrial toxicity. However, the less inert compounds identified in fish and cell toxicity exhibit greatly mitochondrial toxicity. QSAR models reveal that fish or cell toxicity is closely related to the chemical hydrophobicity, ionization, energy of lowest unoccupied molecular orbital, hydrogen bonding potential and stability. These descriptors reflect chemical bio-uptake, reactivity and interaction with target receptors. On the other hand, binomial model reveals that mitochondrial toxicity is closely related to the chemical hydrophobicity and polarizability/dipolarity, indicating bio-uptake and Van der Waals interaction play key roles in mitochondrial toxicity. Theoretical equations have been used to explain the toxicity correlation, excess toxicity and QSAR for fish, cell and mitochondrial toxicity. Above results suggest that cytotoxicity can serve as a surrogate for fish toxicity and be used in the safety evaluation of organic pollutants in aqueous environment, but not mitochondrial toxicity, although some compounds share same modes of action between fish or cell toxicity and mitochondrial toxicity.

Fabrication of Mn/P co-doped hollow tubular carbon nitride by a one-step hydrothermal–calcination method for the photocatalytic degradation of organic pollutants

Efficient photocatalytic degradation of trace organic pollutants in aqueous environment by a hollow tubular carbon nitride co-doped with manganese and phosphorus under visible light.

Photocatalytic Hydrogen Production from Urine Using Sr-Doped TiO2 Photocatalyst with Subsequent Phosphorus Recovery via Struvite Crystallization

Currently, the discharge of wastewater and utilization of phosphorus (P) in human activities cause some environmental problems, such as high organic pollutants in aquatic environments which results in dirty water sources, and a shortage of phosphate rock reserves due to the high demand of P. Therefore, fuel energy and struvite crystallization from waste sources can be considered interesting alternatives. In this work, the modified catalyst for hydrogen production, along with solving environmental problems, was examined. The strontium (Sr) doped-titanium dioxide (TiO2) nanoparticles were synthesized by wetness impregnation method. The synthesized catalyst was characterized using UV-vis spectroscopy (UV-vis), photoluminescence (PL), X-ray diffraction (XRD), photoluminescence (PL), and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS). The Sr-doped TiO2 catalysts had been utilized as the photocatalyst for the hydrogen production from synthetic human urine (a representative of waste source). The doping content of Sr in TiO2 varied from 0.5, 1, 2, and 4%, and the photocatalytic performances were compared with pristine TiO2 nanoparticles. The results showed that 1% Sr-doped TiO2 had the highest photocatalytic activity for hydrogen production and decreased the amount of chemical oxygen demand (COD) in the synthetic human urine. Subsequently, P could be recovered from the treated human urine in the form of struvite.

A nanocubicle-like 3D adsorbent fabricated by in situ growth of 2D heterostructures for removal of aromatic contaminants in water

Focusing on the emergence of organic pollutants in aqueous environments, attempts to assemble two-dimensional (2D) materials into three-dimensional (3D) structures are expected to improve their pollution control performance. However, most 3D heterostructural nanomaterials are constructed by mechanical mixing methods, which result in structures that are randomly arranged and prone to collapse. Two typical 2D carbon materials, reduced graphene oxide (rGO) and covalent triazine frameworks (CTFs), have exhibited excellent effects in the fields of contaminant adsorption and photocatalysis, respectively. However, their regular packing structure could not provide an interconnected pore network suitable for the diffusion or adsorption of pollutants. In this study, a series of heterostructures named rGCs were fabricated by direct growth of 2D CTFs with different ratios on the surface of rGO layers. The rGCs were designed to remove trace concentrations of naphthalene (NAP) and benzophenone (BP) from water, which can be regenerated under sunlight. rGC-20, in which nanocubicle-like 3D heterostructures were successfully constructed, not only adsorbed NAP and BP with superb normalized adsorption capacities (5000–5300 μmol/g) but also could be regenerated with an exceptional percentage recovery of 90–95% in the 4th cycle. The microenvironment created in nanocubicle-like 3D heterostructures enhances the adsorption of pollutants, the excitation of electrons and utilization of radicals, which further promotes the adsorption and photocatalysis of rGCs. This work provides a promising adsorbent with outstanding adsorption-regeneration ability for aromatic contaminant removal from water. Data availabilityThe main data that support the findings of this study are available from the article and its Supplementary Information. Extra data are available from the corresponding author on request.

Emerging organic pollutants in aqueous environments: Detection, monitoring, and removal techniques

Emerging organic pollutants in aqueous environments: Detection, monitoring, and removal techniques

Accelerated photocatalytic degradation of iohexol over Co3O4/g-C3N4/Bi2O2CO3 of p-n/n-n dual heterojunction under simulated sunlight by persulfate

A novel Co3O4/g-C3N4/Bi2O2CO3 (BCCN) photocatalyst with p-n/n-n heterojunction was synthesized through a solvent-thermal method. The degradation efficiency of 20 mg/L iohexol reached 94 % in 60 min (kapp =0.0417 min−1) in BCCN/light/PS system, which was 2.8 and 6.5 times higher than systems of BCCN/light (kapp =0.0150 min−1) and BCCN/PS (kapp =0.0064 min−1). The g-C3N4 addition lowered conduction band of the prepared material to produce superoxide radicals, activate persulfate and further prevent the recombination of photoelectrons and holes. Superoxide radicals and singlet oxygens were dominant radicals for iohexol degradation. Besides, persulfate could act as electron acceptor to enhance efficiency of electron transfer. The interaction between sulfate, superoxide and hydroxyl radicals improved singlet oxygens production. Furthermore, theoretical calculation and liquid chromatography mass spectrometry were performed to analyze degradation pathway of iohexol in the system. Ultimately, the BCCN/light/PS system can provide a new method to degrade organic pollutants in aquatic environments.