tio2与ZnO催化剂多相光催化脱除万古霉素B的比较

G. Lofrano, C. B. Özkal, M. Carotenuto, S. Meriç
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引用次数: 2

摘要

水生生态系统和持久性结构的持续投入引起了对抗生素的关注,主要是由于抗菌素耐药性的潜在发展。研究了自然pH条件下TiO2和ZnO纳米粒子光催化降解万古霉素B (VAN-B)的动力学和矿化过程。通过光催化(PC)效率、紫外吸光度、总有机碳(TOC)和高效液相色谱(HPLC)结果来更好地监测VAN-B本身的降解情况。在多灯间歇式反应器系统(200 mL水体积)中,以2种初始VAN-B浓度(20-50 mg -1)和不同浓度(0.1和0.5 mg -1)的TiO2和ZnO为催化剂,进行了实验。此外,还对大水蚤进行了一组毒性试验,以评估VAN-B氧化副产物的潜在毒性。对氯化物和硝酸盐等中间产物的形成进行了监测。在ZnO-PC体系中观察到快速的VAN-B降解(在10分钟内达到85%至70%),而总的矿化速度相对慢于TiO2-PC体系(在90分钟内达到59%至73%)。处理效率和降解机制直接影响处理样品中产生毒性的转化速率和副产物的形成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of TiO 2 and ZnO catalysts for heterogenous photocatalytic removal of vancomycin B
Continuous input into the aquatic ecosystem and persistent structures have created concern of antibiotics, primarily due to the potential for the development of antimicrobial resistance. Degradation kinetics and mineralization of vancomycin B (VAN-B) by photocatalysis using TiO2 and ZnO nanoparticles was monitored at natural pH conditions. Photocatalysis (PC) efficiency was followed by means of UV absorbance, total organic carbon (TOC), and HPLC results to better monitor degradation of VAN-B itself. Experiments were run for two initial VAN-B concentrations (20–50 mgL-1) and using two catalysts TiO2 and ZnO at different concentrations (0.1 and 0.5 gL-1) in a multi-lamp batch reactor system (200 mL water volume). Furthermore, a set of toxicity tests with Daphnia magna was performed to evaluate the potential toxicity of oxidation by-products of VAN-B. Formation of intermediates such as chlorides and nitrates were monitored. A rapid VAN-B degradation was observed in ZnO-PC system (85 % to 70 % at 10 min), while total mineralization was observed to be relatively slower than TiO2-PC system (59 % to 73 % at 90min). Treatment efficiency and mechanism of degradation directly affected the rate of transformation and by-products formation that gave rise to toxicity in the treated samples.
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