tetracycline has been researched along with peroxymonosulfate* in 22 studies
1 review(s) available for tetracycline and peroxymonosulfate
1 trial(s) available for tetracycline and peroxymonosulfate
21 other study(ies) available for tetracycline and peroxymonosulfate
Article | Year |
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Underwater bubbling plasma assisted with persulfate activation for the synergistic degradation of tetracycline hydrochloride.
The performance and mechanism of persulfate consisting of peroxymonosulfate (PMS) and peroxydisulfate (PDS) activation by underwater bubbling plasma (UBP) for the synergistic removal of tetracycline hydrochloride (TCH) were comparatively investigated. Both PMS and PDS addition significantly promoted the removal of TCH in UBP system, indicating persulfate exhibited highly synergistic effect with UBP. Furthermore, enhancing the persulfate dosage, peak voltage and pulse frequency, as well as reducing initial TCH concentration were favorable for the elimination of TCH. Compared with neutral condition, acidic and alkaline condition were advantageous to TCH removal. The presence of coexisting substances including Cl Topics: Hydrogen Peroxide; Oxidation-Reduction; Peroxides; Tetracycline; Water Pollutants, Chemical | 2024 |
Insight into enhanced degradation of tetracycline over peroxymonosulfate activated via biochar-based nanocomposite: performance and mechanism.
Rice husk biochars (BCs) doped with ferric chloride were prepared by one-pot method, characterized by SEM, EDS, BET, XRD, and FTIR, and utilized to catalyze peroxymonosulfate (PMS) for tetracycline (TC) degradation. Various influencing factors in the BC/PMS/TC system were investigated, as well as the recycling performance of the optimal BC. The mechanism of BC activation of PMS and degradation of TC were analyzed based on the free radicals quenching experiment and the pathways of TC degradation. The results demonstrated that bBC3 was an excellent catalyst with large specific surface area; the amounts of oxidant and catalyst were important factors affecting the catalytic performance of PMS, while pH had less effect on TC degradation; 10 mM of chloride ions inhibited the TC degradation, while 20 mM promoted the TC degradation; other ions and humic acid inhibited the TC degradation at the set concentrations; activation of PMS by bBC3 yielded species with strong oxidative activity, which were primarily responsible for TC degradation. The bBC3 obtained stable performance for removing TC. This study provided a pathway for the deep utilization of waste rice husks besides an effective method for degrading TC. Topics: Anti-Bacterial Agents; Charcoal; Nanocomposites; Peroxides; Tetracycline | 2023 |
An anode fabricated by Co electrodeposition on ZIF-8/CNTs/CF for peroxymonosulfate (PMS) activation.
Topics: Anti-Bacterial Agents; Electrodes; Electroplating; Nanotubes, Carbon; Oxygen; Peroxides; Reactive Oxygen Species; Tetracycline | 2023 |
Fe-N co-doped coral-like hollow carbon shell toward boosting peroxymonosulfate activation for efficient degradation of tetracycline: Singlet oxygen-dominated non-radical pathway.
Fe-N co-doped coral-like hollow carbon shell (Fe-N-CS) was synthesized via a simply impregnation-pyrolysis method. The Fe-N-CS showed an excellent ability for activating peroxymonosulfate (PMS), which could degrade about 93.74% tetracycline (20 mg/L) in 12 min. The Fe-N-CS/PMS system exhibited a good anti-interference capacity of various pH, inorganic anions, HA and different water qualities. More importantly, the Fe nanoparticles were anchored uniformly in the carbon layer, effectively limiting the metal leaching. The quenching tests and electron spin resonance (ESR) manifested that non-radical singlet oxygen ( Topics: Animals; Anthozoa; Anti-Bacterial Agents; Carbon; Heterocyclic Compounds; Reactive Oxygen Species; Singlet Oxygen; Tetracycline | 2023 |
Peroxymonosulfate activation by nitrogen-doped herb residue biochar for the degradation of tetracycline.
Topics: Anti-Bacterial Agents; Charcoal; Nitrogen; Peroxides; Tetracycline | 2023 |
Ultrafast short-range catalytic pathway modified peroxymonosulfate activation over CuO with surface oxygen defects for tetracycline hydrochloride degradation.
Topics: Anti-Bacterial Agents; Ecosystem; Humans; Oxygen; Peroxides; Tetracycline; Water | 2023 |
Insight into radical-nonradical coupling activation pathways of peroxymonosulfate by Cu
In this work, a heterogeneous catalyst of Cu Topics: Anti-Bacterial Agents; Metal-Organic Frameworks; Oxygen; Peroxides; Tetracycline | 2023 |
Efficient degradation of tetracycline residues in pharmaceutical wastewater by Ni/Fe bimetallic atomic cluster composite catalysts with enhanced electron transfer pathway.
Metal cluster catalysts have large atomic load, interaction between atomic sites, and wide application of catalysis. In this study, a Ni/Fe bimetallic cluster material was prepared by a simple hydrothermal method and used as an efficient catalyst to activate the degradation system of peroxymonosulfate (PMS), which showed nearly 100% tetracycline (TC) degradation performance over a wide pH range (pH = 3-11). The results of electron paramagnetic resonance test, quenching experiment and density functional theory (DFT) calculation show that the non-free radical pathway electron transfer efficiency of the catalytic system is effectively improved, and a large number of PMS are captured and activated by high density Ni atomic clusters in Ni/Fe bimetallic clusters. The degradation intermediates identified by LC/MS showed that TC was efficiently degraded into small molecules. In addition, the Ni/Fe bimetallic cluster/PMS system has excellent efficiency for degrading various organic pollutants and practical pharmaceutical wastewater. This work opens up a new way for metal atom cluster catalysts to efficiently catalyze the degradation of organic pollutants in PMS systems. Topics: Anti-Bacterial Agents; Catalysis; Electrons; Environmental Pollutants; Peroxides; Pharmaceutical Preparations; Tetracycline; Wastewater | 2023 |
Activation of peroxymonosulphate using a highly efficient and stable ZnFe
Tetracycline (TC) is a widely used antibiotic that adversely affects ecosystems and, therefore, must be removed from the environment. Owing to their strong ability to oxidise pollutants, including antibiotics, and selectivity for these pollutants, an improved oxidation method based on sulphate radicals (SO4· Topics: Anti-Bacterial Agents; Ecosystem; Environmental Pollutants; Heterocyclic Compounds; Tetracycline | 2023 |
Bamboo charcoal fiber bundles loaded MOF-derived magnetic Co/CoO porous polyhedron for efficiently catalytic degradation of tetracyclines hydrochloride.
The health of living things and the ecosystem of the planet have both been negatively impacted by antibiotic residue in the water environment. There has been a lot of interest in the catalyst made of metal-carbon compounds from MOFs as a potential solution for activating peroxymonosulfate (PMS) to produce reactive oxygen species to catalyze the degradation of residual antibiotics. In this study, zeolitic imidazolate frameworks (ZIF-67) on bamboo fiber bundles (BFB) were pyrolyzed to produce magnetic Co/CoO nanoparticles with porous polyhedrons mounted on bamboo charcoal fiber bundles (BCFB)(BCFB@PCo/CoO). Specific surface area of obtained BCFB@PCo/CoO with abundant active sites arrives at 302.41 m2/g. The catalytic degradation efficiency of Tetracycline hydrochloride (TCH), a target contaminant, could reach up to 99.94% within 15 minutes (PMS = 0.4g/L, Cat. = 0.2g/L). The effects of potential factors, including PMS dosage, interference ions, and temperature, on catalytic degradation efficiencies were investigated. Magnetic recovery and antimicrobial properties of the BCFB@PCo/CoO were also evaluated and the possible degradation pathways were explored. Catalytic mechanism explorations of BCFB@PCo/CoO/PMS system reveal MOF-derived magnetic Co/CoO nanoparticles embedded in BCFB promote the synergistic interaction of both radicals and non-radical pathways for catalytic degradation of TCH. The novel BCFB@PCo/CoO provides an alternative to deal with wastewater containing antibiotics. Topics: Anti-Bacterial Agents; Charcoal; Ecosystem; Magnetic Phenomena; Peroxides; Porosity; Tetracycline | 2023 |
N, S co-doped magnetic mesoporous carbon nanosheets for activating peroxymonosulfate to rapidly degrade tetracycline: Synergistic effect and mechanism.
Heteroatoms doped carbon materials are widely used in the advanced oxidation process (AOPs) to remove organic pollutants in water due to the synergies effect between different heteroatoms. In this study, a novel kind of N, S co-doped magnetic mesoporous carbon nanosheets (Fe@NS-C) was prepared by simple one-step pyrolysis. Further, the influence of doping amount of S (L-methionine) and N (melamine) on catalytic activity was studied, the optimized sample Fe@NS-C-2-12/PMS showed a satisfying degradation ( 91.07%) for high concentrations of tetracycline (80 mg/L TC) in 10 min, which was attributed to the proper ratio of S content to N content (S(at.%)/ N(at.%)= 0.2097) in the sample could better play its synergistic effect by XPS analysis. The Fe@NS-C-2-12/ PMS system also exhibited satisfactory degradation effects in a wide pH range (3-10) and the existence of inorganic ions and humic acid. Then, the degradation mechanisms were mainly through the non-radical pathway ( Topics: Carbon; Magnetic Phenomena; Peroxides; Tetracycline | 2022 |
Insights into the mechanism of enhanced peroxymonosulfate degraded tetracycline using metal organic framework derived carbonyl modified carbon-coated Fe
Tetracycline (TC) is a commonly used antibiotic that has gained wide spread notoriety owing to its high environmental risks. In this study, rich carbonyl-modified carbon-coated Fe Topics: Anti-Bacterial Agents; Carbon; Metal-Organic Frameworks; Peroxides; Tetracycline | 2022 |
Oxidative degradation of tetracycline using peroxymonosulfate activated by cobalt-doped pomelo peel carbon composite.
Tetracycline (TC) is a typical ecotoxic antibiotic, which easily causes bacterial resistance. Therefore, it is necessary to remove TC from the water environment. In recent years, advanced oxidation processes (AOPs) rely on the use of highly reactive oxidizing sulfate radical which is turning into an increasingly popular as a tool of the removal of TC. In this study, cobalt-doped pomelo peel carbon composite (Co-PPCC) was prepared by the impregnation coprecipitation method to activate peroxymonosulfate (PMS) to remove TC. SEM, BET, XRD, FTIR, XPS, TGA, and other analytical techniques indicated that a carbon composite catalyst with excellent performance has been successfully prepared. TC was removed by the synergistic effect of adsorption and catalytic degradation processes. The adsorption capacity was limited (only approximately 20% within 60 min) and tending to saturation, which indicated that the removal of TC in the Co-PPCC/PMS system was mainly due to oxidative degradation. The influence of the Co-PPCC and PMS dosage, initial TC concentration, initial pH values, and coexisting anions on the removal efficiency of TC was investigated. When the Co-PPCC catalyst dosage was 1 g/L, PMS concentration was 2 g/L, and pH value was 11, the removal efficiency of TC with a concentration of 50 mg/L reached 99% within 60 min. Free radical quenching experiment and electron paramagnetic resonance (EPR) analysis indicated that the free radical and non-radical degradation processes exist in the Co-PPCC/PMS/TC system. The main degradation products and the possible transformation pathways of TC were explored by LC-MS. In addition, after four cycles of Co-PPCC tests, the removal efficiency of TC can reach 64%. This study provides a new method to reuse abandoned pomelo peels and synthesize an economical and environmentally friendly catalyst for activating peroxymonosulfate to remove TC antibiotics in water. Topics: Anti-Bacterial Agents; Carbon; Catalysis; Cobalt; Oxidation-Reduction; Oxidative Stress; Peroxides; Tetracycline | 2022 |
High efficiency degradation of tetracycline by peroxymonosulfate activated with Fe/NC catalysts: Performance, intermediates, stability and mechanism.
Carbon-based catalysts have the advantages of biological cleaning, eco-friendly and cost-effective in water treatment. While, nitrogen doped biochar promotes the development of non-radical peroxymonosulfate (PMS) activation in environmental remediation. Thus, three-dimensional sponge-like porous Fe and N co-doped biochar (Fe/CN-30) with high catalytic activity for PMS activation was synthesized. In a wide pH range (1-11), the Fe/CN-30 catalyst can efficiently degrade tetracycline (TC) with a small amount of PMS. The non-radical pathways are prominent in the TC decomposition process according to the quenching experiments, electron paramagnetic resonance (EPR) and gas chromatograph-mass spectrometer (GC-MS) analysis, in which the contribution of high-valent iron-oxo species (Fe(IV) = O) was dominant. X-ray photoelectron spectroscopy and reaction kinetic experiments confirmed that the coordination sites of Fe and N in the Fe/CN-30 are the reactive centers for TC degradation. Moreover, the successive addition of low concentration PMS into the system was confirmed to favor the PMS utilization, and the high selectivity of the Fe/CN-30 was confirmed by the analysis of pollutant structure. Furthermore, by-products of TC degradation in the Fe/CN-30/PMS system and the possible TC degradation pathways were proposed via liquid chromatography-mass spectrometry (LC-MS). Therefore, this study dedicates to providing new insights into the non-radical pathway-catalyzed AOPs. Topics: Anti-Bacterial Agents; Catalysis; Peroxides; Tetracycline | 2022 |
Efficient degradation of tetracycline by singlet oxygen-dominated peroxymonosulfate activation with magnetic nitrogen-doped porous carbon.
Nonradical reaction driven by peroxymonosulfate (PMS) based advanced oxidation processes has drawn widespread attention in water treatment due to their inherent advantages, but the degradation behavior and mechanism of organic pollutants are still unclear. In this study, the performance, intermediates, mechanism and toxicity of tetracycline (TC) degradation were thoroughly examined in the constructed magnetic nitrogen-doped porous carbon/peroxymonosulfate (Co-N/C-PMS) system. The results showed that 85.4% of TC could be removed within 15 min when Co-N/C and PMS was simultaneously added and the degradation rate was enhanced by 3.4 and 14.7 folds compared with Co-N/C or PMS alone, respectively. Moreover, the performance of Co-N/C was superior to that of most previously reported catalysts. Many lines of evidence indicated that Co-N/C-PMS system was a singlet oxygen-dominated nonradical reaction, which was less interfered by pH and water components, and displayed high adaptability to actual water bodies. Subsequently, the degradation process was elaborated on the basis of three-dimensional excitation-emission matrix spectra and liquid chromatography-mass spectrometry. At last, the toxicity of treated TC was greatly reduced by using microalgae Coelastrella sp. as ecological indicator. This study provides a promising approach based on singlet oxygen-dominated nonradical reaction for eliminating TC in water treatment. Topics: Carbon; Magnetic Phenomena; Nitrogen; Peroxides; Porosity; Singlet Oxygen; Tetracycline | 2022 |
How Nitrogen and Sulfur Doping Modified Material Structure, Transformed Oxidation Pathways, and Improved Degradation Performance in Peroxymonosulfate Activation.
Current research has widely applied heteroatom doping for the promotion of catalyst activity in peroxymonosulfate (PMS) systems; however, the relationship between heteroatom doping and stimulated activation mechanism transformation is not fully understood. Herein, we introduce nitrogen and sulfur doping into a Co@rGO material for PMS activation to degrade tetracycline (TC) and systematically investigate how heteroatom doping transformed the activation mechanism of the original Co@rGO/PMS system. N was homogeneously inserted into the reduced graphene oxide (rGO) matrix of Co@rGO, inducing a significant increase in the degradation efficiency without affecting the activation mechanism transformation. Additionally, S doping converted Co Topics: Anti-Bacterial Agents; Cobalt; Graphite; Nitrogen; Oxides; Peroxides; Sulfur; Tetracycline | 2022 |
Enhanced degradation of tetracycline in water over Cu-doped hematite nanoplates by peroxymonosulfate activation under visible light irradiation.
Topics: Ferric Compounds; Light; Peroxides; Tetracycline; Water | 2021 |
Heterogeneous activation of peroxymonosulfate by cobalt-doped MIL-53(Al) for efficient tetracycline degradation in water: Coexistence of radical and non-radical reactions.
Compared with the transition metal induced homogeneous catalytic system, the heterogeneous catalytic system based on transition metal-doped metal organic frameworks (MOFs) were stable for the efficient utilization of transition metal and avoiding the metal leaching. The aim of this work is to synthesize Co-doped MIL-53(Al) by one-step solvent thermal method and use it to activate peroxymonosulfate (PMS) to remove tetracycline (TC) in water. The successful synthesis of Co-MIL-53(Al) samples was demonstrated by XDR, SEM and FTIR characterizations. The 25% Co-MIL-53(Al)/PMS system showed the optimal TC removal effect compared to the PMS alone and MIL-53(Al)/PMS system. The catalytic performances of Co-MIL-53(Al)/PMS system in conditions of different pH, co-existing substances and water bodies were investigated. Quenching experiment and electron paramagnetic resonance (EPR) showed that the degradation mechanism by Co-MIL-53(Al) activation PMS was mainly attributed to sulfate radical (SO Topics: Cobalt; Peroxides; Tetracycline; Water | 2021 |
Cobalt-impregnated biochar (Co-SCG) for heterogeneous activation of peroxymonosulfate for removal of tetracycline in water.
Cobalt-impregnated spent coffee ground biochar (Co-SCG) was synthesized and applied for tetracycline (TC) removal from water. The results showed that Co-SCG biochar exhibited marked adsorption capacity and catalyst activity. The maximum adsorption capacity of Co-SCG biochar toward TC was 370.37 mg g Topics: Charcoal; Cobalt; Peroxides; Tetracycline; Water; Water Pollutants, Chemical | 2019 |
Efficient degradation of tetracycline by ultraviolet-based activation of peroxymonosulfate and persulfate.
Topics: Anti-Bacterial Agents; Oxidation-Reduction; Peroxides; Photochemical Processes; Sulfates; Tetracycline; Ultraviolet Rays; Water Pollutants, Chemical | 2019 |
Sonocatalytic degradation of tetracycline antibiotic using zinc oxide nanostructures loaded on nano-cellulose from waste straw as nanosonocatalyst.
Topics: Anti-Bacterial Agents; Catalysis; Cellulose; Nanocomposites; Oxidants; Peroxides; Tetracycline; Ultrasonic Waves; Water; Water Pollutants, Chemical; Zinc Oxide | 2019 |