Antibiotic Pollution Research Articles

Interactions between microplastics and organic contaminants: the microbial mechanisms for priming effects of organic compounds on microplastic biodegradation

The co-presence of plastics and other organic contaminants is pervasive in various ecosystems, particularly in areas with intensive anthropogenic activities. Their interactions inevitably impact the composition and functions of the plastisphere microbiome, which in turn determines the trajectory of these contaminants. Antibiotics are a group of organic contaminants that warrant particular attention due to their wide presence in environments and significant potential to disseminate antibiotic resistance genes (ARGs) within the plastisphere. Therefore, this study investigated the impacts of sulfadiazine (SDZ), a prevalent environmental antibiotic, on the composition and function of the plastisphere microbial community inhabiting micro-polyethylene (mPE), one of the most common microplastic contaminants. Our findings indicated that the presence of SDZ increased the overall plastisphere microbial abundance and enriched populations that are capable of degrading both SDZ and mPE. The abundance of Aquabacterium, a dominant plastisphere population that is capable of degrading both SDZ and mPE, increased over the course of SDZ exposure, while another abundant mPE-degrading population, Ketobacter, remained stable. Accordingly, the removal of SDZ was enhanced in the presence of mPE. Moreover, the results further revealed that not only SDZ but also other labile organic contaminants (e.g., aniline and hexane) could accelerate mPE biodegradation through a priming effect. This investigation underscores the complex dynamics among microplastics, organic contaminants, and the plastisphere microbiome, offering insights into the environmental fate of plastic and antibiotic pollutants.

Enhanced Tetracycline Adsorption Using KOH-Modified Biochar Derived from Waste Activated Sludge in Aqueous Solutions.

Antibiotic pollution poses a serious environmental concern worldwide, posing risks to ecosystems and human well-being. Transforming waste activated sludge into adsorbents for antibiotic removal aligns with the concept of utilizing waste to treat waste. However, the adsorption efficiency of these adsorbents is currently limited. This study identified KOH modification as the most effective method for enhancing tetracycline (TC) adsorption by sludge biochar through a comparative analysis of acid, alkali, and oxidant modifications. The adsorption characteristics of TC upon unmodified sludge biochar (BC) as well as KOH-modified sludge biochar (BC-KOH) were investigated in terms of equilibrium, kinetics, and thermodynamics. BC-KOH exhibited higher porosity, greater specific surface area, and increased abundance of oxygen-based functional groups compared to BC. The TC adsorption on BC-KOH conformed the Elovich and Langmuir models, with a maximum adsorption capacity of 243.3 mg/g at 298 K. The adsorption mechanisms included ion exchange, hydrogen bonding, pore filling, and electrostatic adsorption, as well as π-π interactions. Interference with TC adsorption on BC-KOH was observed with HCO3-, PO43-, Ca2+, and Mg2+, whereas Cl-, NO3-, and SO42- ions exhibited minimal impact on the adsorption process. Following three cycles of utilization, there was a slight 5.94% reduction in the equilibrium adsorption capacity, yet the adsorption capacity remained 4.5 times greater than that of unmodified sludge BC, underscoring its significant potential for practical applications. This research provided new insights to the production and application of sludge biochar for treating antibiotic-contaminated wastewater.

Enhanced Antibiotic Pollutant Capture: Coupling Carbon Nanotubes with Covalent Organic Frameworks

Enhanced Antibiotic Pollutant Capture: Coupling Carbon Nanotubes with Covalent Organic Frameworks

Electrostatic self-assembly of hydrotalcite-based g-C3N4 composites for adsorption and photocatalytic degradation of aqueous norfloxacin

Norfloxacin, a quinolone antibiotic pollutant, posed a significant threat to environment and human being health. In this study, hydrotalcite-based g-C3N4 composites were produced using electrostatic self-assembly and the structural memory effect of hydrotalcite to optimize their adsorption-degradation of norfloxacin under visible-light illumination. Optimized hydrotalcite and g-C3N4 composite (750°C, 40 wt% of g-C3N4) exhibited a highest photo-degradation rate constant of 1.8×10−2 min−1 with 83.98 % norfloxacin degradation achieved within 1.5 h under visible-light, surpassing that of bare g-C3N4 and hydrotalcite photocatalysts. The synergistic effects of the composite, such as uniform flower-like micro-morphology and rich mesoporous structure, resulted in a large specific surface area (58.67 m2/g), abundant active sites, and good photo-generated charge separation efficiency. All these facilitated both sorption (7.95 mg/g) and subsequent visible-light degradation of norfloxacin. Furthermore, the superior photocatalytic performance observed in the degradation of norfloxacin under visible-light illumination was assigned to the effective transport of photogenerated electrons and holes between hydrotalcite and g-C3N4 components. The work highlights the potentials of hydrotalcite and g-C3N4 composites as an excellent photocatalyst for environment remediation and water treatment.

Trace iron induced piezo-polarization field strength on piezo-promoted peroxymonosulfate activation for pollutant degradation

Advanced oxidation processes based on piezo-promoted peroxymonosulfate (PMS) activation in environmental remediation have been widely applied, but the treatment efficiency of pollutants was restricted by sluggish charge separation and low affinity of PMS. Herein, trace iron-doped layered molybdenum disulfide (Fe/MoS2) was used to degrade pollutants by piezo-promoted PMS activation. Real-time reaction site changes in carbamazepine (CBZ) degradation process were predicted by Fukui function calculation of the reaction intermediates, and the possible degradation pathways were given. Through piezoresponse force microscopy and calculation of the adsorption energy, electronic localized functions and Crystal Orbital Hamilton Population, it was verified that Fe doping improves the adsorption of oxygen-containing reactants on MoS2, enhancing the electron delocalization and piezo-polarization field, thus accelerating the piezo-promoted PMS activation kinetics. The degradation efficiency of CBZ on Fe/MoS2 (0.44 min−1) was about 22 times than that of MoS2. Piezo-promoted PMS activation strategy based on Fe/MoS2 still maintains a high removal rate in the treatment of dye and antibiotic pollutants such as ornidazole, rhodamine B, tetracycline, methyl orange, chlortetracycline. This study provides insights into the mechanism by which piezo-promoted PMS activation, and achieving high chemical efficiency for pollutants removal.

Enhancement in the antibacterial activity of Rifaximin by delivery through gelatin nanoparticles

Objectives Bacterial infections are a noteworthy global health concern that necessitates the development of new strategies to enhance the potency and efficacy of antibiotics. Rifaximin (RFX), a broad-spectrum antibiotic, exhibits promising antibacterial activity against several bacterial strains. However, its insolubility and impermeability impede the exploitation of its full potential. The objective of the current study is to overcome the inherent caveats of RFX to exploit its maximum potential. Significance The exploitation of the full potential of antibiotics is necessary for reduction in their dosage and to minimize antibiotic pollution. This is a preliminary study aiming for maximum utilization of RFX at the target site and reduction in its release in unmetabolized form. Methods Gelatin is a biopolymer that has gained significant attention for biomedical applications owing to its inherent biocompatibility and biodegradability. In this study, bovine gelatin nanoparticles (BGNPs) were fabricated by the self-assembly method for their application as a carrier of RFX to enhance its antibacterial activity. The study employs a comprehensive range of experimental techniques to characterize the fabricated BGNPs such as DLS, Zeta Potential, FT-IR, AFM, SEM-EDX, and UV-Vis spectrophotometry. Results The average size of the fabricated BGNPs was 100 nm with a zeta potential value of −15.3 mV. The loading of RFX on BGNPs rendered an increase in its size to 136 nm with a zeta potential value of −16 mV. In-vitro assays and microscopic analyses were conducted to compare the antibacterial efficacy of RFX and RFX@BGNPs. An excellent loading capacity followed by sustained release of RFX from RFX@BGNPs rendered a significant enhancement in its pharmaceutical efficacy. The release of RFX from RFX@BGNPs followed the Higuchi and Korsmeyer-Peppas models. The antibacterial efficacy of RFX against Staphylococcus aureus has doubled by delivery through RFX@BGNPs, assessed by inhibitory and biofilm inhibitory assays. The enhancement in the antibacterial efficiency was further endorsed by SEM and microscopic imaging of the control and treated bacterial colonies. Conclusion The study demonstrates an enhancement in the antimicrobial efficacy of RFX by its delivery in the form of RFX@BGNPs to exploit its full potential for practical applications.

Regional distribution differences of antibiotics in tropical marine aquaculture area: Insights into antibiotic management and risk assessment

In recent years, global demand for marine aquaculture products has led to a significant rise in antibiotic use, particularly in tropical coastal aquaculture areas However, research on antibiotic residues in these environments remains limited, hindering a comprehensive understanding of their environmental presence and associated risks. This study investigates the regional distribution, ecological risks, and sources of 44 antibiotics in seawater across four coastal aquaculture areas in Hainan island (Wenchang, Sanya, Danzhou, and Wanning). Among the 44 antibiotics tested across 42 sampling sites, all were detected with a 100 % detection rate. Antibiotics such as Trimethoprim (TMP), Sulfanitran (APNPS), Sulfaquinoxaline (SQ), Sulfadimethoxine (SDT), Chloramphenicol (CHP), and Florfenicol (FLO) were consistently detected across all sampling sites. Total concentrations of detected antibiotics ranged from 0 to 818.79 ng.L−1, with sulfonamide antibiotics ranging from 0 to 629.49 ng.L−1, chloramphenicol antibiotics from 0 to 87.39 ng.L−1, tetracyclines from 0 to 221.39 ng.L−1, and fluoquinolones from 0 to 272.08 ng.L−1. The highest levels of antibiotic pollution were observed at the W5 sampling site in Wenchang, attributed to aquaculture wastewater discharge, while no antibiotics were found at D12 in Danzhou. In these regions, source analysis identified aquaculture and domestic sewage as the primary contributors to antibiotic pollution in these regions. Correlation analysis with environmental factors revealed significant influences of factors such as SAL, kPa, TN, SPC, and pH on sulfonamide and chloramphenicol antibiotics. Health risk assessment indicated moderate to high risks to aquatic organisms from antibiotics like NOR, CIP, ENR, OFL, TMP, and SMX in the study areas, underscoring the need for preventive measures, stricter regulation of antibiotic use, and enhanced ecological risk monitoring in aquaculture regions. This study provides critical insights into antibiotic contamination in Hainan's coastal aquaculture areas, highlighting the urgent need for further research into the occurrence and ecological impacts of these emerging pollutants in marine environments.

Effect of sponge city facilities on the exposure characteristics and ecological risks of antibiotics in urban inland lakes: A case study at Fuzhou, China.

Antibiotics are increasingly found in urban lakes, posing significant ecological risks to lake ecosystems. The impact of sponge city facilities on urban flood control is significant; however, their influence on the exposure characteristics and risks associated with antibiotics in urban inland lakes remains unclear. This study investigated the exposure characteristics and evaluated the ecological risks of 15 antibiotics across seven lakes of Fuzhou (as the target of sponge city) in different seasons, in comparison to non-sponge cities. The results revealed that 12 antibiotics were consistently detectable across all lakes, with concentrations ranging from non-detectable (ND) to 20.61ng/L, with sulfamethoxazole (SMX) emerging as the predominant contaminant. Most antibiotics exhibited higher concentrations in the dry season, attributed to environmental conditions, biological mechanisms, and their physicochemical properties. SMX, tetracycline (TTC), oxytetracycline (OTC), and ciprofloxacin (CIP) posed moderate to high ecological risks, with risk quotient (RQ) values of 0.46, 0.14, 0.17, and 0.61, respectively, while the remaining antibiotics presented lower ecological risks in both seasons. Notably, the RQ values for TTC, OTC, and CIP were elevated during the dry season, whereas SMX displayed a higher RQ value in the wet season, indicating an increased ecological risk during the dry months. In comparison to non-sponge cities, sponge cities exhibited significantly lower concentrations of nearly all antibiotics, particularly during the wet season (p ≤ 0.05). Moreover, over 85% of the antibiotics in non-sponge cities were classified as high risk, contrasted with only 55% in sponge cities, underscoring the heightened ecological risks associated with non-sponge urban designs. This study provides critical insights for controlling antibiotic pollution in the lakes of Fuzhou and serves as a valuable reference for maintaining aquatic ecosystem health through the implementation of sponge city infrastructure.

Development of improved technologies for protecting fish from infections in aquaculture

The current intensification of marine aquaculture is inevitably associated with such environmental issues as growing infections and the need to apply antibiotic and other antimicrobial preparations. This leads to antibiotic pollution in the environment. Latest technologies aimed at preventing fish infections in aquaculture are based on the vaccination of the objects under cultivation. These technologies allow the use of antibiotics to be reduced and the balance of the microbial environment in aquaculture to be restored, eventually minimizing the negative effects of antibiotic residues on the human health. In this work, we set out to study molecular mechanisms underlying the immune response of fish to viral infections. Data on the expression of some genes of the most important aquaculture objects in Russia and China in response to infection and during its progression was obtained. The research results can be used when developing vaccines against vibriosis with the purpose of minimizing the application of medical preparations, such as antibiotics. These measures are important for maintaining healthy fish habitats and, as a consequence, the human health.

Degradation mechanism and ecotoxicity analysis of levofloxacin by palladium-modified nano zero-valent iron doped coconut shell biochar

The palladium-modified nano zero-valent iron (nZVI) doped coconut shell biochar (Pd-nZVI/BC) was successfully obtained through bimetallic modification and liquid-phase reduction. The synthesized Pd-nZVI/BC was further enhanced by the addition of an H2O2 co-catalyst for the removal of antibiotic levofloxacin (LVF). Results demonstrated that removal of LVF by Pd-nZVI/BC accomplished 94.6 % under proper conditions. Adsorption and degradation processes were involved in the LVF removal, and the predominant free radicals were •OH and •O2-. Adsorption relied mainly on electrostatic interactions, π-π interactions, and hydrogen bonding. While demethylation, deamidation, quinolone ring aldolization, depiperazinylation, deacetylation, decarboxylation, dehydroxylation, and oxidative breakage of the piperazine ring occurred during the degradation processes. Based on the degradation pathways, the ecotoxicity of LVF and its degradation intermediates were compared and assessed. Results implied that majority of the antibiotic LVF pollutant was eliminated or mineralized, and the toxicity potential of LVF was reduced in the Pd-nZVI/BC system. Simultaneous biochar utilization and pollutants removal could be achieved.

Smart sensing property of Eu3+-induced polyelectrolyte nanoaggregates on nitrofuran antibiotics in aqueous environments

Pollution of water with antibiotics is a very serious global issue. So, simple, fast, and ecofriendly detection of such pollutants in aqueous environments has aroused great attention. Several intriguing properties such as narrow emission band, large stokes shift, long luminescence decay time and resistance to photobleaching distinguishes europium-based materials from commonly used fluorophores in biology as a superior optical smart material for applications in diverse fields. Herein, strongly luminescent Eu3+-induced polyelectrolyte nanoaggregates (EINAP) were synthesized and successfully characterized. The biocompatible polysaccharides hyaluronic acid and chitosan are used to disperse organic europium complexes resulting in formation of hybrid nanoaggregates. As synthesized EINAP demonstrated excellent quantum yield (89.29 %) and luminescence lifetime (656 µs). The EINAP also have high sensitivity and low limit of detection with good analytical precision for nitrofuran antibiotics in aqueous environments. The luminescent nano sensor developed in this work could be a novel tool for assessment of antibiotic pollution in the environment. The overall sensing mechanisms for detection of nitrofurans in aqueous environments were found to be the combination of inner filter effect and photoinduced electron transfer respectively.

Influence of gadolinium substitution on the crystal structure of NiO and its maximized photocatalytic degradation activity on tetracycline and direct yellow pollutants

Gadolinium-substituted NiO crystal structures with excellent stability were utilized for the first time to degrade antibiotic and organic dye pollutants. A simple hydrothermal technique was used to synthesize different concentrations of Gd3+ substituted NiO, and the catalysts were thoroughly characterized using sophisticated techniques to explore the influence of Gd3+ on the crystal structure and optical characteristics of NiO. The 1.5% Gd3+ substituted NiO showed outstanding photocatalytic activity on tetracycline and direct yellow degradation, with percentages of 90.72 and 95.5%, respectively. The improvement of photocatalytic degradation efficiency is primarily due to the suppression of photoinduced electron and hole recombination via the creation of Gd3+ as the inner energy band state below the conduction band. The recycling experiments revealed that the catalyst is more stable, with no indication of loss after ten cycles. Scavenging investigations also demonstrated that superoxide and holes were responsible for the efficient degradation of pollutants.

Tetracycline removal by immobilized indigenous bacterial consortium using biochar and biomass: Removal performance and mechanisms

The significant influx of antibiotics into the environment represents ecological risks and threatens human health. Microbial degradation stands as a highly effective method for reducing antibiotic pollution. This study explored the potential of immobilized microbial consortia to efficiently degrade tetracycline. Concurrently, the suitability of different immobilization materials were assessed, with reed charcoal-immobilized consortia exhibiting the highest efficiency in removing tetracycline (92%). Similarly, wheat-bran-loaded bacterial consortia displayed a remarkable 11.43-fold increase in tetracycline removal compared with free consortia. Moreover, adding the carriers increased the nutrients, while the activities of both intracellular and extracellular catalases increased significantly post-immobilization, thus highlighting this enzyme’s crucial role in tetracycline degradation. Finally, analysis of the microbial communities revealed the prevalence of Achromobacter and Parapedobacter, signifying their potential as key degraders. Overall, the immobilized consortia not only hold promise for application in the bioremediation of tetracycline-contaminated environment but also provide theoretical underpinnings for environmental remediation by microorganisms.

Incorporating C3N5 and NiCo2S4 to Form a Novel Z-Scheme Heterojunction for Superior Photocatalytic Degradation of Norfloxacin

Due to a combination of increased urbanization, industrialization, and population growth, many pharmaceutical pollutants are currently being discharged into the environment. A possible strategy is critical for eliminating antibiotic pollutants from the environment, and photocatalysis has been generally recognized as an excellent method for successfully degrading antibiotics at a faster pace. In this work, we employed a hydrothermal synthesis approach to create a novel C3N5/NiCo2S4 Z-scheme-based heterojunction with better interfacial charge transfer and used it as a catalyst for the degradation of norfloxacin antibiotic. The optimized 1:1 C3N5/NiCo2S4 (50CN/NCS) shows the highest photocatalytic efficiency of 86.5% in 120 min towards the degradation of norfloxacin (NOR). Such an effective performance can be attributed to the high responsive nature of photocatalyst in the visible region and superior transfer of interfacial charges via Z-scheme transfer in heterojunction. The high charge transfer efficiency and reduced recombination of charge carriers in heterojunction was confirmed by EIS and PL results. The influence of some key factors such as pollutant concentration, catalyst dosage, pH, and coexisting ions on the photocatalytic activity is also investigated in this work. The optimized heterojunction 50CN/NCS also degraded 89.1%, 78.3%, and 93.2% removal of the other pollutants CIP, SDZ, and BPA, respectively.

Treatment of antibiotics in mariculture wastewater via phosphate-doped porous coralline carbon nitride/porous mullite honeycomb sunlight-driven photocatalytic system: Morphological control, long-term and continuous flow application

Herein, this study describes a promising sunlight-driven photocatalytic system designed for the elimination of antibiotics (e.g., fluoroquinolones and sulfonamides) in real maricultural wastewater. Phosphate-doped porous coralline carbon nitride (P-CCN), synthesized by controlling morphology from two-dimensional block CN, was immobilized onto porous mullite honeycomb to construct a practical and molding photocatalytic system (P-CCN/PMH). By leveraging its microscopic porous coral structure, P-CCN displayed an augmentation in surface-active sites and a notable inner light refraction effect. This enhancement contributed to the high-efficiency performance of P-CCN/PMH system, producing 8.232 mM·h−1·g−1 H2O2 under sunlight, which was 7.21-fold higher than before modification; and its degradation rate constant to enrofloxacin (0.263 min−1) was 39.31-fold higher. The P-CCN/PMH system demonstrated superior capability in terms of adaptability to a wide concentration range, acid-alkali conditions, mineralization, carbon reduction, and challenging ionic surroundings or water matrices. Crucial superoxide radicals have been confirmed through mass-spectrometric technique and theoretical calculations, leading to ring-opening effects. Long-term and continuous-flow experiments were deeply carried out, validating the commendable competence of the P-CCN/PMH photocatalytic system in simulated wastewater treatment scenarios. Ultimately, the aggregate results highlight valuable insights into coralline materials synthesis and modular catalyst construction, presenting potential for addressing challenges related to environmental antibiotics pollution.

Sustainable photodegradation of pharmaceuticals: KOH-impregnated palm oil mill effluent sludge biochar-BiOBr nanocomposite for wastewater treatment

Biochar has explored in the search of a cost-effective and environmentally friendly photocatalyst for the efficient degradation of CIP antibiotic pollutants. Biochar (BC) produced from palm oil mill sludge was used as a base to fabricate biochar-based BiOBr composites by varying the mass ratio of biochar and BiOBr via a hydrothermal route. The optimized composites BBC-1:1 has exhibited the formation of crystal struvture as tetragonal BiOBr with a a significant specific surface of 267 m2/g (BBC-1:1) while incorporating different mass ratios of BC with BiOBr. This composite facilitates the band gap of BiOBr from 2.87 to 2.42 eV and is consistent with the decreasing recombination rate of electron-hole pairs as suggested by UV-Vis DRS and photoluminescence (PL), respectively. Consequently, the synergistic effect of biochar BiOBr leads to a higher degradation efficiency of CIP showing the highest efficiency (97.49 %) and that of pure BiOBr being 55.66 % under optimized conditions. The degradation rate of the BBC-1:1 composite which observed to be 0.0156 min−1 is 3.25 times that of BiOBr (0.0048 min−1). Furthermore, the scavenging experiments confirmed the significant contribution of the active radicals h+ and O2- as the main photoactive species in the photocatalytic degradation of CIP. Consequently, the photocatalytic degradation mechanism was discussed and the reusability test confirmed the high stability of the BBC composites up to 77 % for the seventh cycles. These results show that the BBC composite is suitable for large-scale practical applications as a green photocatalyst.

Insights into the factors influencing the oxidation of antibiotic pollutants in nitrogen-doped biochar/PMS system: The roles of physicochemical properties and reaction pathways

The advanced oxidation of persulfate catalyzed by nitrogen-doped biochar (NBC) has emerged as a significant area of research, owing to its remarkable efficacy in selectively removing antibiotic organic pollutants from aquatic environments. Despite exhibiting promising results, the comprehension of the selective oxidation mechanisms of NBC remains inadequate, primarily stemming from the intricate complexity of organic pollutants and the vast variety of free radical active species involved. This study aims to elucidate the underlying mechanisms that drive the different oxidation processes promoted by NBC, with a focus on understanding the interactions between the physicochemical properties of various antibiotic contaminants and the resulting oxidation pathways. Regression analysis reveals the significance of adsorption interactions in constructing reaction interfaces, where the molecular polarity, complexity, topological polarity surface area, and molecular weight of pollutants play pivotal roles. However, these parameters do not singularly dictate the oxidation process. Instead, the electrochemical properties of organic pollutants (open-circuit potential, half-wave potential, and molecular orbital energy) primarily determine the selective oxidation. Furthermore, the research highlights that free radicals contribute to the oxidation of pollutants with relatively weak electrochemical properties, such as norfloxacin, but are insufficient to drive the entire oxidation process. Conversely, for pollutants with strong electrochemical properties, such as ofloxacin and oxytetracycline, the influence of free radicals is negligible. Overall, the study seeks to provide insights into the roles of adsorption interactions, electrochemical properties, and free radical dynamics, thereby advancing the development of efficient and targeted strategies for environmental remediation.

Screening of Characteristic Pollutants and Risk Pollutants in Different Media in the Yangtze River Basin Using Comprehensive Evaluation and Risk Quotient Methods

A variety of pollutants have frequently been detected in the Yangtze River Basin with the rapid economic development, the population increase, and the acceleration of urbanization, which threaten the aquatic ecosystem and human health. A multi-criteria comprehensive evaluation method was developed to identify the characteristic pollutants, and the risk quotient method was used to derive the risk pollutants in water and sediment samples in this article. A total of 155 pollutants from 11 categories were detected in the Yangtze River Basin according to the literature research. Then, the K-means method was used to analyze the cluster of pollutant comprehensive scores. All pollutants were graded based on their scores and recorded as Ⅰ-Ⅵ according to the number of cases in each cluster. A total of 43 pollutants with high scores of Ⅰ and Ⅱ were listed as the characteristic pollutants, which included 11 polycyclic aromatic hydrocarbons, 11 organochlorine pesticides, 10 polychlorinated biphenyls, eight dioxins, two heavy metals, and one phthalate ester. The top five median concentrations of contaminants in water and sediment samples were heavy metals, polycyclic aromatic hydrocarbons, phthalates esters, bisphenols, and pharmaceuticals and personal care products. According to the principle of risk maximization, the risk entropy value （RQ） was calculated based on the highest pollutant concentration. A total of 38 risky pollutants were screened in the water samples （RQ ≥ 0.1）. There were eight high-risk pollutants with RQ ≥ 1, which included benzo[a,h]-anthracene, anthracene, benzo[a]anthracene, pyrene, methoxychlor, aldrin, 2,4'-dichlorodiphenyl, and cadmium. There were 15 high-risk contaminants in the sediment, which included benzo[b]fluoranthene, anthracene, acenaphthene, fluoranthene, cadmium, lead, chromium, arsenic, selenium, dibutyl phthalate, dimethyl phthalate, diisobutyl phthalate, norfloxacin, perfluorobutyric acid, and bisphenol A. The risk pollutants contained emerging pollutants, which included ten pollutants in water samples and nine pollutants in sediments. Antibiotic pollutants accounted for the largest proportion of these emerging pollutants. The information provided in this article may be useful for the relevant departments to monitor the pollutants and propose management programs for the Yangtze River Basin. Additionally, it is of great significance for the ecological environmental protection and management of the Yangtze River Basin.

Advanced Z-scheme H-g-C3N4/Bi2S3 nanocomposites: Boosting photocatalytic degradation of antibiotics under visible light exposure

Abnormal concentrations of antibiotics found in aquatic environments have raised serious environmental concerns. For the efficient degradation of antibiotics, it is necessary to develop photocatalysts that react to visible light. In this work, calcination and hydrothermal methods were used to synthesize bare H-g-C3N4 and Bi2S3, respectively. Various analytic methods, such as XRD, XPS, FT-IR, HR-SEM, and HR-TEM, were utilized to verify the accomplished synthesis of the materials produced. The results of ultraviolet–visible diffuse reflectance spectroscopy (UV–DRS) showed that the synthesized nanocomposites exhibited a lower band gap than the bare materials and thus greater visible-light absorption. The degradation efficacy of the bare materials and hydrothermally synthesized nanocomposites over ciprofloxacin were investigated. A high degradation efficiency of 92 % was demonstrated for ciprofloxacin using the H-g-C3N4/Bi2S3 (5 %) nanocomposite. This remarkable efficiency underscores the potential of this nanocomposite in removing antibiotic pollutants from wastewater. In addition, the electron transfer dynamics amid the two materials (H-g-C3N4 and Bi2S3) within the heterojunction was elucidated. The findings provide valuable insights into the mechanisms underlying the enhanced photocatalytic activity of nanocomposites, paving the way for further optimization and development of advanced photocatalytic systems for environmental remediation.

Antibiotics pollutants in agricultural soil: Kinetic, sorption, and thermodynamic of ciprofloxacin

The entry of antibiotics, as pollutants, into the environment has created great concerns. Environmental dynamics of antibiotics based on soil chemical properties need to be a better understanding of their chemical behavior. This research is focused on studying the adsorption behavior and kinetic mechanisms of ciprofloxacin (CIP) in an agricultural soil. For this purpose, a batch experiment was conducted at different times (5 min–24 h), and using initial concentrations of CIP (0–1 mmol L−1) in the soil. The adsorption processes as affected by pH and ionic strength were assessed based on the modeling with response surface methodology (RSM). According to the results, the sorption equilibrium was found within 240 min, and the pseudo second-order model was the best for describing the data. Increasing the initial CIP concentration increased CIP adsorption, but increases in ionic strength and pH had an inverse effect. Based on RSM modeling, the CIP adsorption was 7.31 and 7.03 (mg g−1) in the presence of NaCl and CaCl2 electrolytes, respectively, in the optimized conditions (pH 6.5 and ionic strength 0.01 mol L−1). The spontaneous nature of CIP adsorption was determined based on thermodynamic calculations (ΔG° = −10.8 to −12.4 kJ mol−1). The interaction of pH and ionic strength was described with the quadratic model. The obtained results contribute to understanding the CIP fate in the soil environment and facilitate decisions regarding entry and controlling soil contamination due to this antibiotic.