Enhanced photodegradation of oxytetracycline antibiotic in wastewater by implementing ZnO-loaded carbon fiber.

The antibiotic oxytetracycline (OCA) exhibits high insolubility in the natural environment, posing a significant challenge for its removal. This study synthesized a porous structure and a high-surface-area carbon fiber, incorporating zinc oxide (ZnO/CFB) for the effective removal of OCA in wastewater. The material characterization revealed exceptional optical and photochemical properties of ZnO/CFB, featuring a reduced band gap energy of 2.7 eV. ZnO/CFB exhibited robust performance in the photodegradation of OCA in wastewater, achieving an impressive removal efficiency of 86.7%. Remarkably, the reduction of total organic carbon (TOC) reached an outstanding 97.5%. LC-MS analysis confirmed the complete oxidation of OCA and its intermediates, transforming them into inorganic substances within 60 min. This study introduces an efficient strategy for eliminating antibiotic pollutants from wastewater, highlighting the potential of ZnO/CFB as an effective and stable photocatalyst for environmental remediation.

Photocatalytic degradation of oxytetracycline hydrochloride pollutants in marine aquaculture wastewater under visible light.

A CuO/ZnO nanocomposite for use as photocatalyst was successfully prepared by co-precipitation method. Its chemical and physical properties were evaluated by X-ray diffractometry, scanning electron microscopy, EDS, UV-vis diffuse reflectance spectroscopy and photoluminescence spectroscopy. The average particle size of CuO/ZnO composite was found to be around 80 nm. The degradation of oxytetracycline hydrochloride pollutants in marine aquaculture wastewater using ZnO and CuO/ZnO was compared. CuO/ZnO nanocomposite was found to be more efficient than ZnO. The effects of external factors on the photocatalytic efficiency of the nanocomposite were investigated under visible light. Moreover, conditions for the degradation of oxytetracycline hydrochloride using CuO/ZnO nanocomposite were optimized. Based on both, the ability and efficiency of degradation, 10:1 molar ratio of Zn2+/Cu2+ and 0.4 g L-1 nanocomposite, were found to be optimal, using which the average photocatalytic degradation rate of oxytetracycline hydrochloride reached 90%.

MoS2-based nanocomposites and aerogels for antibiotic pollutants removal from wastewater by photocatalytic degradation process: A review.

Photocatalytic technologies based on molybdenum disulfide (MoS2) catalysts are effective, eco-friendly, and promising for antibiotic pollutants treatment. The technologies used by MoS2-based nanocomposites and aerogels for efficient degradation of antibiotics are reviewed in detail for the first time in this paper. The fundamental aspects of MoS2 were comprehensively scrutinized, encompassing crystal structure, optical properties, and photocatalytic principle. Then, the main synthesized methods and advantages/disadvantages for the preparation of MoS2-based nanocomposites and aerogels were systematically presented. Besides, a comprehensive overview of diverse MoS2-based nanocomposites and aerogels photo-degradation systems that enhanced the degradation of antibiotic pollutants were revealed. Meanwhile, the photo-degradation mechanism concentrated on the photoelectron transfer pathways and reactive oxygen species (ROS) were systematically evaluated. Finally, the challenges and perspectives for deeply development of MoS2-based nanocomposites and aerogels were discussed. This review may help researchers to deeply understand the research status of MoS2-based nanocomposites and aerogels for antibiotics removal, and makes clear the photo-degradation mechanism from photoelectron transfer pathways and ROS aspects of MoS2-based nanocomposites and aerogels.

Efficacy of new generation biosorbents for the sustainable treatment of antibiotic residues and antibiotic resistance genes from polluted waste effluent.

Antimicrobials are frequently used in both humans and animals for the treatment of bacterially-generated illnesses. Antibiotic usage has increased for more than 40% from last 15 years globally per day in both human populations and farm animals leading to the large-scale discharge of antibiotic residues into wastewater. Most antibiotics end up in sewer systems, either directly from industry or healthcare systems, or indirectly from humans and animals after being partially metabolized or broken down following consumption. To prevent additional antibiotic compound pollution, which eventually impacts on the spread of antibiotic resistance, it is crucial to remove antibiotic residues from wastewater. Antibiotic accumulation and antibiotic resistance genes cannot be effectively and efficiently eliminated by conventional sewage treatment plants. Because of their high energy requirements and operating costs, many of the available technologies are not feasible. However, the biosorption method, which uses low-cost biomass as the biosorbent, is an alternative technique to potentially address these problems. An extensive literature survey focusing on developments in the field was conducted using English language electronic databases, such as PubMed, Google Scholar, Pubag, Google books, and ResearchGate, to understand the relative value of the available antibiotic removal methods. The predominant techniques for eliminating antibiotic residues from wastewater were categorized and defined by example. The approaches were contrasted, and the benefits and drawbacks were highlighted. Additionally, we included a few antibiotics whose removal from aquatic environments has been the subject of extensive research. Lastly, a few representative publications were identified that provide specific information on the removal rates attained by each technique. This review provides evidence that biosorption of antibiotic residues from biological waste using natural biosorbent materials is an affordable and effective technique for eliminating antibiotic residues from wastewater.

[Occurrence and environmental risks of antibiotics in surface water of China].

Antibiotics as emerging pollutants are frequently detected in surface water, raising concerns about the associated risk of antibiotic resistance genes (ARGs). Despite the widespread apprehension, there are still research gaps in the occurrence of antibiotic pollution in surface water and the associated ecological risks to aquatic organisms in China. Here, we established a dataset of antibiotic pollution in surface water in China during 2018-2022, which encompassed 3 368 concentration values of 128 antibiotics reported in 124 articles. Our analysis showed that antibiotic concentrations were predominantly in the ng/L-µg/L range, reaching up to 26 µg/L. Notably, sulfonamides (e.g., sulfamethoxazole) and quinolones (e.g., ciprofloxacin) were frequently reported at high concentrations. The pollution degree of antibiotics represented by sulfamethoxazole, ciprofloxacin, roxithromycin, and tetracycline exhibited no significant variation across different years but was lower in summer than that in spring and autumn. Additionally, distinct spatial distribution characteristics of the pollution were observed. According to calculation results of the aquatic ecological risk assessment model and the weighted frequency, we proposed a list of priority antibiotics including clarithromycin, erythromycin, sulfamethoxazole, ofloxacin, and oxytetracycline in surface water. Last but not least, this study points out the deficiencies in current research on the occurrence and ecological risks of antibiotics in surface water of China and provides viable screening strategies and monitoring recommendations in this context.

Evaluating the Combined Effects of Erythromycin and Levofloxacin on the Growth of Navicula sp. and Understanding the Underlying Mechanisms.

Navicula sp., a type of benthic diatom, plays a crucial role in the carbon cycle as a widely distributed algae in water bodies, making it an essential primary producer in the context of global carbon neutrality. However, using erythromycin (ERY) and levofloxacin (LEV) in medicine, livestock, and aquaculture has introduced a new class of pollutants known as antibiotic pollutants, which pose potential threats to human and animal health. This study aimed to investigate the toxic effects of ERY and LEV, individually or in combination, on the growth, antioxidant system, chlorophyll synthesis, and various cell osmotic pressure indexes (such as soluble protein, proline, and betaine) of Navicula sp. The results indicated that ERY (1 mg/L), LEV (320 mg/L), and their combined effects could inhibit the growth of Navicula sp. Interestingly, the combination of these two drugs exhibited a time-dependent effect on the chlorophyll synthesis of Navicula sp., with ERY inhibiting the process while LEV promoted it. Furthermore, after 96 h of exposure to the drugs, the activities of GSH-Px, POD, CAT, and the contents of MDA, proline, and betaine increased. Conversely, the actions of GST and the contents of GSH and soluble protein decreased in the ERY group. In the LEV group, the activities of POD and CAT and the contents of GSH, MDA, proline, and betaine increased, while the contents of soluble protein decreased. Conversely, the mixed group exhibited increased POD activity and contents of GSH, MDA, proline, betaine, and soluble protein. These findings suggest that antibiotics found in pharmaceutical and personal care products (PPCPs) can harm primary marine benthic eukaryotes. The findings from the research on the possible hazards linked to antibiotic medications in aquatic ecosystems offer valuable knowledge for ensuring the safe application of these drugs in environmental contexts.

Preparation of TiO2/Fe-MOF n‒n heterojunction photocatalysts for visible-light degradation of tetracycline hydrochloride.

Visible-light-assisted photocatalysis has been recognized as an effective solution to the degradation of various pollutants including antibiotics, pesticides, herbicides, microplastics, and organic dyes. Herein, an n-n heterojunction TiO2/Fe-MOF photocatalyst is reported, designed via solvothermal synthesis route. TiO2/Fe-MOF photocatalyst was characterized by XPS, BET, EIS, EDS, DRS, PL, FTIR, XRD, TEM, SEM and HRTEM techniques. Inspired by XRD, FTIR, XPS, EDS, TEM, SEM, and HRTEM analyses, the successful synthesis of n-n heterojunction TiO2/Fe-MOF photocatalysts was proved. The migration efficiency of the light-induced electron-hole pairs was confirmed by the PL and EIS tests. TiO2/Fe-MOF exhibited a significant performance for tetracycline hydrochloride (TC) removal under visible light irradiation. TC removal efficiency for TiO2/Fe-MOF (15%) nanocomposite reached 97% within 240 min, ca. 11 times higher than pure TiO2. The photocatalytic enhancement of TiO2/Fe-MOF could be attributed to the broadening the light response range, forming an n-n junction between Fe-MOF and TiO2 components, suppressing charge recombination. Based on recycling experiments, TiO2/Fe-MOF had a good potential to be used in consecutive TC degradation tests.

Photodegradation of ciprofloxacin antibiotic in water by using ZnO-doped g-C3N4 photocatalyst.

Ciprofloxacin antibiotic (CIP) is one of the antibiotics with the highest rate of antibiotic resistance, if used and managed improperly, can have a negative impact on the ecosystem. In this research, ZnO modified g-C3N4 photocatalyst was prepared and applied for the decomposition of CIP antibiotic compounds in water. The removal performance of CIP by using ZnO/g-C3N4 reached 93.8% under pH 8.0 and an increasing amount of catalyst could improve the degradation performance of the pollutant. The modified ZnO/g-C3N4 completely oxidized CIP at a low concentration of 1 mg L-1 and the CIP removal efficiency slightly decreases (around 13%) at a high level of pollutant (20 mg L-1). The degradation rate of CIP by doped sample ZnO/g-C3N4 was 4.9 times faster than that of undoped g-C3N4. The doped catalyst ZnO/g-C3N4 also displayed high reusability for decomposition of CIP with 89.8% efficiency remaining after 3 cycles. The radical species including ·OH, ·O2- and h+ are important in the CIP degradation process. In addition, the proposed mechanism for CIP degradation by visible light-assisted ZnO/g-C3N4 was claimed.

Facile Fabrication of Novel NiFe2O4@Carbon Composites for Enhanced Adsorption of Emergent Antibiotics.

Water purification is becoming one of the most pertinent environmental issues throughout the world. Among common types of water pollution involving heavy metals, pharmaceutical drugs, textile dyes, personal care products, and other persistent organic pollutants, the pollution of antibiotic drugs is increasingly emerging due to their adverse effects on microorganisms, aquatic animals, and human health. Therefore, the treatment of such contaminants is very necessary to reduce the concentration of antibiotic pollutants to permissible levels prior to discharge. Herein, we report the use of NiFe2O4@C composites from a bimetallic-based metal-organic framework Ni-MIL-88B(Fe) for removal of ciprofloxacin (CFX) and tetracycline (TCC). The effect of production temperatures (600-900 °C), solution pH (2-10), NiFe2O4@C dose (0.05-0.2 g/L), concentration of antibiotics (10-60 mg/L), and uptake time (0-480 min) was investigated systematically. Response surface methodology and central composite design were applied for quadratic models to discover optimum conditions of antibiotic adsorption. With high coefficients of determination (R2 = 0.9640-0.9713), the proposed models were significant statistically. Under proposed optimum conditions, the adsorption capacity for CFX and TCC were found at 256.244, and 105.38 mg/g, respectively. Recyclability study was employed and found that NiFe2O4@C-900 could be reused for up to three cycles, offering the potential of this composite as a good adsorbent for removal of emergent antibiotics.

Visible-light-driven photocatalytic removal of antibiotics by newly designed C3N4@MnFe2O4-graphene nanocomposites.

Newly designed magnetic g-C3N4/MnFe2O4/graphene (C3N4@MnFe2O4-G) composites with enhanced photocatalytic activity were successfully synthesized. The photocatalytic behavior of C3N4@MnFe2O4-G was assessed in photo Fenton-like degradation of antibiotic pollutants, including metronidazole, amoxicillin, tetracycline and ciprofloxacin, using persulfate (S2O82-) as an oxidant under visible light illumination. The C3N4@MnFe2O4-G composites show a superior catalytic activity with 94.5% removal of metronidazole that was almost 3.5 times as high as that of the pure g-C3N4, which could be attributed to the synergistic promoting effect of the favorable adsorptivity, enhanced light absorption intensity, high migration efficiency of charge carriers and longer lifetime of separated electron-hole pairs derived from the formation of the heterojunction between the g-C3N4 and MnFe2O4. Moreover, the self-redox properties of iron and manganese atoms in MnFe2O4 induced by S2O82- were particularly beneficial for the generation of SO4-. The quenching tests and electron spin resonance (ESR) display that h+, O2-, SO4- and OH are responsible for the antibiotics decomposition. The heterogeneous photocatalyst could be easily recovered by an extra magnetic field and reused several times without any obvious deterioration in catalytic activity. According to the investigation of active species and identified intermediates, the possible photocatalytic mechanism and reaction pathways have been proposed.

Identification of new transformation products during enzymatic treatment of tetracycline and erythromycin antibiotics at laboratory scale by an on-line turbulent flow liquid-chromatography coupled to a high resolution mass spectrometer LTQ-Orbitrap.

This work describes the formation of transformation products (TPs) by the enzymatic degradation at laboratory scale of two highly consumed antibiotics: tetracycline (Tc) and erythromycin (ERY). The analysis of the samples was carried out by a fast and simple method based on the novel configuration of the on-line turbulent flow system coupled to a hybrid linear ion trap - high resolution mass spectrometer. The method was optimized and validated for the complete analysis of ERY, Tc and their transformation products within 10 min without any other sample manipulation. Furthermore, the applicability of the on-line procedure was evaluated for 25 additional antibiotics, covering a wide range of chemical classes in different environmental waters with satisfactory quality parameters. Degradation rates obtained for Tc by laccase enzyme and ERY by EreB esterase enzyme without the presence of mediators were ∼78% and ∼50%, respectively. Concerning the identification of TPs, three suspected compounds for Tc and five of ERY have been proposed. In the case of Tc, the tentative molecular formulas with errors mass within 2 ppm have been based on the hypothesis of dehydroxylation, (bi)demethylation and oxidation of the rings A and C as major reactions. In contrast, the major TP detected for ERY has been identified as the "dehydration ERY-A", with the same molecular formula of its parent compound. In addition, the evaluation of the antibiotic activity of the samples along the enzymatic treatments showed a decrease around 100% in both cases.