研究目的
To investigate the degradation of tetracycline (TTC) in water using the medium pressure UV-activated peroxymonosulfate (MPUV/PMS) process, including influencing factors, degradation pathways, and toxicity evaluation.
研究成果
MPUV/PMS is an efficient method for TTC degradation, with ?OH as the main active species. Factors like higher PMS dosage, pH, and presence of Cl- and CO32- enhance degradation. However, incomplete mineralization leads to toxic transformation products, increasing genotoxicity initially. Further research is needed to mitigate toxicity risks.
研究不足
The study did not achieve complete mineralization of TTC, as indicated by negligible TOC removal. Toxicity increased initially due to formation of toxic transformation products, highlighting potential environmental risks. The use of real water samples showed improved degradation but may involve complex interactions with water constituents not fully explored.
1:Experimental Design and Method Selection:
The study used a bench-scale quasi-collimated beam system with a medium-pressure UV lamp to activate peroxymonosulfate (PMS) for degrading TTC. Radical quenching and competitive kinetics experiments were employed to identify active species and rate constants.
2:Sample Selection and Data Sources:
TTC solutions were prepared in Milli-Q water and real sand-filtered waters. Samples were collected at various UV doses for analysis.
3:List of Experimental Equipment and Materials:
Equipment included a MPUV lamp (Philips,
4:8 kW), quasi-collimated beam system, UV radiometer (IL1700, International Light), spectrophotometer (Beijing Persee TU-1901), HPLC system (LD-20A, Shimadzu), UPLC/Q-TOF MS system (Waters ACQUITY UPLC and XEVO G2 Q-TOF), and materials such as TTC, PMS (Oxone salt), scavengers (TBA, EtOH), and buffers. Experimental Procedures and Operational Workflow:
Batch experiments were conducted by irradiating samples in a petri dish, adjusting pH with NaOH and H2SO4, varying PMS dosage, pH, and anion concentrations. Samples were analyzed for TTC concentration, transformation products, and toxicity.
5:Data Analysis Methods:
Data were analyzed using pseudo-first-order kinetics for degradation rates, competitive kinetics for rate constants, and QSAR software (ECOSAR and T.E.S.T) for toxicity prediction.
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