Degradation Of Tetracycline Antibiotics Research Articles

Study on the Effect of Conditioners on the Degradation of Tetracycline Antibiotics in Deer Manure Composting

The unscientific disposal of agricultural solid waste introduces more antibiotics and other pollutants into the environment. Composting, as an environmentally friendly solid waste disposal method, can be used as a green way to degrade antibiotics, and conditioners can regulate the physicochemical indicators of the composting process. This article investigates the removal mechanism of tetracycline antibiotics (TCs) during the composting process by adding different regulators (biochar, zeolite, and biochar + zeolite). The results showed that the conditioning agent could significantly improve the removal efficiency and removal rate of TCs in compost. Among them, the addition of the zeolite group had the highest degradation rate of TCs, which were 91.39% (Tetracycline), 97.18% (Chlortetracycline), and 95.68% (Oxytetracycline). The combination of biochar and zeolite conditioning agents effectively minimized the migration of TCs into the soil. According to the findings of the artificial neural network model, it was determined that TCs exhibited the highest sensitivity to biochar + zeolite modulators at 31.28%. Conditioners influenced the removal of TCs in compost by impacting their physicochemical properties and microbial community structure. We isolated and domesticated a suitable microbial preparation that promotes the degradation of TCs, including Acinetobacter pittii, Stenotrophomonas maltophilia, Lactobacillus reuteri, Pseudomonas putida, and Trichosporon dohaense.

Dual purpose of graphene decorated with Cu3SnS4 as a counter electrode for dye sensitized solar cells and degradation of tetracycline antibiotics

Dual purpose of graphene decorated with Cu3SnS4 as a counter electrode for dye sensitized solar cells and degradation of tetracycline antibiotics

Recent Advances in Photocatalytic Degradation of Tetracycline Antibiotics

China is a significant global producer and consumer of pesticides and antibiotics, with their excessive use leading to substantial water pollution that poses challenges for subsequent treatment. Photocatalytic degradation, leveraging renewable solar energy, presents an effective approach for decomposing organic pollutants and reducing residual contaminant levels in water bodies. This approach represents one effective way for addressing environmental challenges. This paper classifies representative photocatalytic materials by structural design and degradation principles including MOFs (Metal–Organic Frameworks), metal- and nonmetal-doped, mesoporous material-loaded, carbon quantum dot-modified, floatation-based, and heterojunction photocatalysts. We also discuss research on degradation pathways and reaction mechanisms for antibiotics. Of particular importance are several key factors influencing degradation efficiency, which are summarized within this work. These include the separation and charge transfer rate of catalyst surface carriers, and the wide-spectrum response capabilities of photocatalysts, as well as persulfate activation efficiency. Furthermore, emphasis is placed on the significant role played by intrinsic driving forces such as built-in electric fields within catalytic systems. Moreover, this paper introduces several promising composite-structure photocatalytic technologies from both composite-structure perspectives (e.g., Aerogel-based composites) and composite-method perspectives (e.g., the molecularly imprinted synthesis method). We also discuss their latest development status, along with future prospects, presenting valuable insights for pollutant degradation targets. This work aims to facilitate the design of efficient photocatalytic materials, while providing valuable theoretical references for environmental governance technologies.

Construction of Co-Modified MXene/PES Catalytic Membrane for Effective Separation and Degradation of Tetracycline Antibiotics in Aqueous Solutions.

The application of antibiotics has advanced modern medicine significantly. However, the abuse and discharge of antibiotics have led to substantial antibiotic residues in water, posing great harm to natural organisms and humans. To address the problem of antibiotic degradation, this study developed a novel catalytic membrane by depositing Co catalysts onto MXene nanosheets and fabricating the polyethersulfone composite (Co@MXene/PES) using vacuum-assisted self-assembly. The dual role of MXene as both a carrier for Co atoms and an enhancer of interlayer spacing led to improved flux and catalytic degradation capabilities of the membrane. Experimental results confirmed that the Co@MXene/PES membrane effectively degraded antibiotics through peroxymonosulfate activation, achieving up to 95.51% degradation at a cobalt concentration of 0.01 mg/mL. The membrane demonstrated excellent antibacterial properties, minimal flux loss after repeated use, and robust anti-fouling performance, making it a promising solution for efficient antibiotic removal and stable water treatment.

Single-atom Ru modified flake g-C3N4 enhances photogenerated electron transport for rapid degradation of tetracycline antibiotics: Non-radical mechanism and ecotoxicity studies

Design of green and low-cost single-atom catalysts (SACs) with high-performance is key to moving photocatalytic degradation of antibiotics toward applications. In order to achieve SACs for large-scale manufacturing, we prepared ultrathin flake carbon nitride (FCN) by low-energy-consuming physical knockout means, and also applied an in situ growth strategy with stable and easy-operating effect to anchor the Ru element on FCN in the form of single atom. Notably, in the PMS/Vis/0.5Ru-FCN system, the degradation rate of tetracycline achieved 100 % in just five minutes, with an apparent rate constant of 0.236 min−1. Ru-FCN exhibits selective and stable determination due to narrow bandgap, unique photoresponsivity and low photogenerated carrier complexation rate. Mechanism investigation reveal that Ru-N4 sites accelerated the electron transfer between Ru-FCN and PMS, while the low oxidation state of Ru elements reduced the risk for metal corrosion. DFT calculations predict the attack sites of reactive oxygen species. This work provides a rational explanation for the charge transfer and resistance to external disturbance by Ru single atom, and it also provides a new direction to enhance the efficiency of water treatment.

Degradation Of Tetracycline Antibiotic in Water by an Electro/Peroxydisulfate System Catalyzed with Fe2+ and Cu2+ Loaded on Activated Carbon

Degradation Of Tetracycline Antibiotic in Water by an Electro/Peroxydisulfate System Catalyzed with Fe2+ and Cu2+ Loaded on Activated Carbon

Extended Interfacial Charge Transference in CoFe2O4/WO3 Nanocomposites for the Photocatalytic Degradation of Tetracycline Antibiotics.

The large-scale utilization of antibiotics has opened a separate chapter of pollution with the generation of reactive drug-resistant bacteria. To deal with this, in this work, different mass ratios of CoFe2O4/WO3 nanocomposites were prepared following an in situ growth method using the precursors of WO3 and CoFe2O4. The structure, morphology, and optical properties of the nanocomposite photocatalysts were scrutinized by X-ray diffraction (XRD), UV-visible diffuse reflectance spectra (UV-Vis DRS), photoluminescence spectrum (PL), etc. The experimental data signified that the loading of CoFe2O4 obviously changed the optical properties of WO3. The photocatalytic performance of CoFe2O4/WO3 composites was investigated by considering tetracycline as a potential pollutant. The outcome of the analyzed data exposed that the CoFe2O4/WO3 composite with a mass ratio of 5% had the best degradation performance for tetracycline eradication under the solar light, and a degradation efficiency of 77% was achieved in 20 min. The monitored degradation efficiency of the optimized photocatalyst was 45% higher compared with the degradation efficiency of 32% for pure WO3. Capturing experiments and tests revealed that hydroxyl radical (·OH) and hole (h+) were the primary eradicators of the target pollutant. This study demonstrates that a proper mass of CoFe2O4 can significantly push WO3 for enhanced eradication of waterborne pollutants.

Simple synthesis of 2D/3D mpg-C3N4/ZnO nanocages with built-in driven Z-scheme heterostructures: Photocatalytic degradation of tetracycline antibiotics and lifting the limitation of the complex water environment

Tetracycline antibiotics have attracted attention due to their difficulty in being degraded by the natural environment. In this work, 2D/3D mesoporous graphitic carbon nitride (mpg-C3N4)/ zinc oxide (ZnO) hollow nanocage (MCNZH) complexes with Z-scheme heterostructure were prepared for the photocatalytic degradation of tetracycline antibiotics. The catalysts were characterized by SEM, TEM, BET, XRD, FT-IR, EIS, etc. The degradation of tetracycline hydrochloride (40 mg L–1) by MCNZH (1.2 g L–1) can reach 92.08 %. Further, the energy band structure of the catalysts were calculated and the possible degradation mechanism was proposed. The results showed that ·OH– and ·O2– were the main active species, and the internal electric field suppressed the compounding of photogenerated carriers. The catalysts exhibited broad-spectrum degradation of tetracycline antibiotics. Practical sample spiking experiments on soil and river water confirmed its practicability, which provide great significance for the application of the photocatalytic technology in the practical environmental purification.

Bifunctional Pt-loaded steel slag matrix composites for the detection and degradation of tetracycline antibiotics

In this paper, a method for the simultaneous detection and degradation of tetracycline antibiotics (TCs) in water was investigated. Calcium silicate hydrate (CSH), FeO and calcium aluminate hydrate (CAH) were isolated from steel slag as carriers for Pt monomers. The produced Pt-modified modified steel slag (ALANH-Pt) possessed both peroxidase activity and photocatalytic properties. As a result, a sensitive and selective colorimetric sensor was exploited on the basis of ALANH-Pt for tetracycline (TC), oxytetracycline (OTC), and doxycycline (DOX), which exhibited a detection limit (LOD) of 1.696 μM, 0.999 μM and 3.607 μM, respectively. In addition, the degradation rate for TCs could be achieved 82 % within 60 min. The possible mechanisms of detection and degradation are discussed based on ESR spectroscopy, revealing the generation of hydroxyl radicals (OH), superoxide radicals (O2−) and holes (h+). The degradation pathway of TC was inferred by HPLC-MS. The selectivity of the colorimetric sensing platform and the application of the bifunctional ALANH-Pt to real water samples were investigated. This work provides a new idea that allows for the simultaneous detection and degradation of TCs, and offers a new approach to the utilization of steel slag.

Fe-doped TiO2/PVDF-HFP electrospun membranes for tetracycline photocatalytic degradation under visible light

Heterogeneous photocatalysis operated under visible light is considered an efficient and ecofriendly method to remove pharmaceuticals from water streams. However, the recovery of the nano-sized catalyst particles limits this technology to small-scale applications. In this study, we prepared Fe-doped P25 TiO2 photocatalysts and immobilized them over PVDF-HFP electrospun membranes for the photocatalytic degradation of Tetracycline antibiotic under visible light. To ensure uniform distribution of the nanoparticles on the fibers, the electrospinning voltage and the weight percentage of TiO2 were varied, and two preparation methods were applied to disperse the catalyst in the polymeric solution. In order to maximize the visible light exposure of the membranes, 3D printed membrane holders with square and circular shapes were designed to immerse the membrane in Tetracycline solution. The results showed that immobilizing P25 catalysts on the fibers of the membranes limited their visible light absorption when the light source was assembled on the top of the aqueous reaction medium. This occurred due to the membrane's opacity limited light penetration, resulting in uneven irradiation throughout its depth. Based on this, a new photocatalytic reactor design was proposed with immersed light illumination source to reduce the distance between the membrane and the light source for improved activation of the P25 particles. In this design, a 3D-printed vertical membrane holder was also included to accommodate a larger membrane surface area and therefore minimize the required spatial area for large industrial applications.

Microbial Degradation of Tetracycline Antibiotics: Mechanisms and Environmental Implications.

The escalating global consumption of tetracyclines (TCs) as broad-spectrum antibiotics necessitates innovative approaches to mitigate their pervasive environmental persistence and associated risks. While initiatives such as China's antimicrobial reduction efforts highlight the urgency of responsible TC usage, the need for efficient degradation methods remains paramount. Microbial degradation emerges as a promising solution, offering novel insights into degradation pathways and mechanisms. Despite challenges, including the optimization of microbial activity conditions and the risk of antibiotic resistance development, microbial degradation showcases significant innovation in its cost-effectiveness, environmental friendliness, and simplicity of implementation compared to traditional degradation methods. While the published reviews have summarized some aspects of biodegradation of TCs, a systematic and comprehensive summary of all the TC biodegradation pathways, reactions, intermediates, and final products including ring-opening products involved with enzymes and mechanisms of each bacterium and fungus reported is necessary. This review aims to fill the current gap in the literature by offering a thorough and systematic overview of the structure, bioactivity mechanism, detection methods, microbial degradation pathways, and molecular mechanisms of all tetracycline antibiotics in various microorganisms. It comprehensively collects and analyzes data on the microbial degradation pathways, including bacteria and fungi, intermediate and final products, ring-opening products, product toxicity, and the degradation mechanisms for all tetracyclines. Additionally, it points out future directions for the discovery of degradation-related genes/enzymes and microbial resources that can effectively degrade tetracyclines. This review is expected to contribute to advancing knowledge in this field and promoting the development of sustainable remediation strategies for contaminated environments.

Sonocatalytic performance of Bi2WO6 nanoparticles for degradation of tetracycline antibiotics

Sonocatalytic performance of Bi2WO6 nanoparticles for degradation of tetracycline antibiotics

Facile synthesis of MIL-88A/PVA sponge for rapid tetracycline antibiotics degradation via sulfate radical-advanced oxidation processes

MIL-88A is a metal–organic framework (MOF) material known for its excellent performance in advanced oxidation processes (AOPs). However, due to its powdery nature, MIL-88A may undergo loss during catalytic degradation in flowing solutions, making continuous degradation removal challenging. Herein, we report the synthesis of MIL-88A/PVA sponge composite material by the in-situ integration of MIL-88A with PVA sponge. The composite sponge exhibits excellent removal efficiency of tetracycline antibiotics under the conditions of sulfate radical-advanced oxidation processes (SR-AOPs), achieving a degradation rate exceeding 99.0% within 2 min. Additionally, through fixed-bed column experiments, 1 kg of MIL-88A/PVA can treat 2160 L of wastewater within 24 h, indicating promising industrial applicability. It’s worth noting that this material can be customized into any desired block shape as needed. This work offers a highly promising solution for the application of MOF-based bulk-type catalysts in the treatment of antibiotic pollution using SR-AOPs.

Floating MIL-88A(Fe)@expanded perlites catalyst for continuous photo-Fenton degradation toward tetracyclines under artificial light and real solar light

In this work, MIL-88A(Fe) was immobilized onto the expanded perlites to fabricate the floating MIL-88A(Fe)@expanded perlites (M@EP) catalyst via high throughput batch synthesis method under room temperature. The as-prepared M@EP could efficiently activate H2O2 to achieve 100% tetracycline antibiotics (TCs) removal under both artificial low power UV light (UVL) and real sunlight (SL) irradiation. The toxicological evaluation, growth experiment of mung beans and antimicrobial estimation revealed the decreasing aquatic toxicity of the TCs intermediates compared to those of the pristine TCs. A self-designed continuous bed reactor was employed to investigate the long-term operation of the M@EP. The findings demonstrated that the antibiotics mixture can be continuously degraded up to 7 days under UVL and 5 daytimes under SL irradiation, respectively. More importantly, ca. 76.9% and 81.6% of total organic carbon (TOC) removal efficiencies were accomplished in continuous bed reactor under UVL and SL irradiation, respectively. This work advances the immobilized MOFs on floating supports for their practical application in large-scale wastewater purification through advanced oxidation processes. Environmental implicationThis work presented the high throughput production and photo-Fenton degradation application of floating MIL-88A(Fe)@expanded perlites (M@EP). Three tetracycline antibiotics (TCs) were selected as model pollutants to test the degradation ability of M@EP in batch experiment and continuous operation under artificial light and solar light. The complete TCs degradation could be accomplished in self-designed device up to 7 d under UV light and 5 d under real solar light. This work tapped a new door to push MOFs-based functional materials in the real water purification.

Ultrasmall Cu2O@His with laccase- and catechol oxidase-like activity: Applications in phenolic drug identification and degradation

Nanozymes constitute a category of nanomaterials exhibiting the potential to replace natural enzymes. Although many types of nanozymes have been widely reported in different fields, fabricating nanozymes with ultrasmall dimensions and expanding their applications is still a great challenge. In this study, we present a cost-effective, one-step methodology for producing ultrasmall Cu2O@His. Comparative to natural laccases, Cu2O@His demonstrates remarkable catalytic capabilities in phenolic catalysis, alongside robust stability and economic viability. Therefore, some potential applications of Cu2O@His as an alternative to natural laccase were explored. Cu2O@His has been utilized not only for the detection of epinephrine but also for the degradation of tetracycline antibiotics. In addition, four kinds of TCs were successfully distinguished by principal component analysis. This work provides new ideas and methods for the development of nanozymes with ultrasmall dimensions and for the study of applications of laccase-like activity.

Efficient photocatalytic degradation of tetracycline antibiotic and melachite green dye using La-BDC MOFs

Efficient photocatalytic degradation of tetracycline antibiotic and melachite green dye using La-BDC MOFs

Interface engineering in a nitrogen-rich COF/BiOBr S-scheme heterojunction triggering efficient photocatalytic degradation of tetracycline antibiotics

Tetracycline (TC) antibiotics, extensively utilized in livestock farming and aquaculture, pose significant environmental challenges. Photocatalysis, leveraging renewable sunlight and reusable photocatalysts, offers a promising avenue for mitigating TC pollution. However, identifying robust photocatalysts remains a formidable challenge. This study introduces a novel hollow-flower-ball-like nanoheterojunction composed of a nitrogen-rich covalent organic framework (N-COF) coupled with BiOBr (BOB), a semiconductor with a higher Fermi level. The synthesized N-COF/BOB S-scheme nanoheterojunction features an expanded contact interface, strengthened chemical bonding, and unique band topologies. The N-COF/BOB composites showcased exceptional TC degradation performance, achieving an 81.2% removal of 60 mg/L TC within 2 h, markedly surpassing the individual efficiencies of N-COF and BOB by factors of 3.80 and 5.96, respectively. Furthermore, the total organic carbon (TOC) removal efficiency highlights a superior mineralization capacity in the N-COF/BOB composite compared to the individual components, N-COF and BOB. The toxicity assessment revealed that the degradation intermediates possess diminished environmental toxicity. This enhanced performance is ascribed to the robust S-scheme nanoheterojunction structure, which promotes efficient photoinduced electron transfer from BOB to N-COF. This process also augments the separation of photogenerated charge carriers, resulting in an increased yield of superoxide radicals (∙O2−) and hydroxyl radicals (∙OH). These reactive species significantly contribute to the degradation and mineralization of TC. Consequently, this study introduces a sustainable approach for addressing emerging antibiotic contaminants, employing COF-based photocatalysts.

Bifunctional activation of peroxymonosulfate over CuS/g-C3N4 composite for efficient degradation of tetracycline antibiotics

Graphitic carbon nitride (g-C3N4) modified by CuS was fabricated for efficient bifunctional activation of peroxymonosulfate (PMS) and degradation of tetracycline (TC) in water. On the one hand, PMS could be activated by metal ions, and reducing sulfur species as electron donors, promoting the Cu(Ⅰ)/Cu(Ⅱ) cycle. On the other hand, under visible light excitation, CuS and g-C3N4 recombination significantly improved the separation efficiency of electron hole pairs, and electrons effectively migrated to PMS, generating more ROSs. The removal efficiency of TC reached 97.46 % in the optimal configuration. In addition, the 35 % CuS/g-C3N4/PMS/Light system exhibited excellent degradation ability of TC in different water matrix. The combination of free radicals (O2•−, •OH and SO4•−) and non-free radical (1O2) pathways enhanced the degradation of TC, in accordance with scavenging experiments and electron paramagnetic resonance (EPR) analysis. Density functional theory (DFT) calculations supported the higher adsorption energy of PMS on CuS/g-C3N4 composite in comparison to pure materials. Overall, this work demonstrates the practical relevance of CuS/g-C3N4/PMS/Light system for the efficient degradation of TC in the application of environmental remediation, offering an innovative approach for diminishing refractory organics and wastewater treatment expenses.

Fabrication of a Z-scheme Bi2MoO6/NiFe layered double hydroxide heterojunction for the visible light-driven degradation of tetracycline antibiotics

Heterojunction catalysts offer promising potential for efficient and sustainable remediation of polluted environments. In this study, Z-scheme Bi2MoO6/NiFe layered double hydroxide (BMO/NiFe) heterojunction catalysts were synthesized using solvothermal process. The surface morphology, crystalline structure, and photochemical characteristics of the synthesized photocatalyst were analyzed by several spectroscopic and electron microscopy methods. BMO, NiFe and BMO/NiFe were efficiently utilized for tetracycline (TC) antibiotics degradation under visible light irradiation. The experimental findings suggest that the BMO/NiFe15 heterojunction catalyst greatly enhances the TC degradation rate to 95 % under 300 W visible light irradiation for 120 min. The rate constant of 0.0219 min−1 indicates a rapid degradation process following pseudo first-order kinetics. Furthermore, the effect of active free radicals, the recyclability of the catalyst and the photocatalytic degradation mechanism of TC were proposed. This novel method opens up possibilities for creating advanced photocatalysts, which can effectively degrade TC in water bodies, addressing the urgent need for its removal from aquatic environments. The present work serves as a primary pathway to design and develop efficient Bi2MoO6-based direct Z-scheme photocatalysts with promising applications in simultaneous wastewater degradation with hydrogen evolution.

Construction of a continuous packed bed laccase reactor for the elimination of tetracyclines in seawater

Tetracycline antibiotics (TCs) are extensively present in the marine environment and have adverse effects on human health and aquatic ecosystems. Laccases are a type of green biocatalyst for TCs degradation. In this study, a continuous packed bed reactor based on the immobilized modified laccase was constructed to degrade TCs at environmentally relevant levels in seawater. Results showed that the chemical modification and immobilization of laccase had a synergistic effect on its activity and stability in seawater: after incubation in seawater for 12 h, the residual activity of free laccase was only 22.3%, while that of the immobilized modified laccase (A/PhA-Lac) was 79.3%. A laccase reactor was constructed based on A/PhA-Lac, and the response surface regression model was established to optimize the laccase reactor operating conditions. The laccase reactor under optimal conditions could continuously degrade TCs (5 μg/L each) in seawater within 10 h and reach the highest removal rate at 4 to 5 h (removal rates of tetracycline, oxytetracycline, and chlorotetracycline were 94.7%, 86.6% and 98.0%, respectively). The luminescent bacteria microtoxicity and seawater microbial community analysis revealed that the laccase reactor significantly mitigated the toxicity of TCs in seawater. This study provided an environmentally friendly and effective method for the elimination of antibiotics in seawater.