首页> 外文期刊>The Science of the Total Environment >Efficient cephalexin degradation using active chlorine produced on ruthenium and iridium oxide anodes: Role of bath composition, analysis of degradation pathways and degradation extent
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Efficient cephalexin degradation using active chlorine produced on ruthenium and iridium oxide anodes: Role of bath composition, analysis of degradation pathways and degradation extent

机译:使用钌和氧化铱阳极制备的活性氯的高效头碱素降解:浴组成的作用,降解途径分析和降解程度

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The elimination of cephalexin (CPX) using electro-generated Cl-2-active on Ti/RuO2-IrO2 anode was assessed in different effluents: deionized water (DW), municipal wastewater (MWW) and urine. Single Ti/RuO2 and Ti/IrO2 catalysts were prepared to compare their morphologies and electrochemical behavior against the binary DSA. XRD and profile refinement suggest that Ti/RuO2-IrO2 forms a solid solution, where RuO2 and IrO(2 )growths are oriented by the TiO2 substrate through substitution of Ir by Ru atoms within its rutile-type structure. SCM reveals mud-cracked structures with flat areas for all catalysts, while EDS analysis indicates atomic ratios in the range of the oxide stoichiometries in the nominal concentrations used during synthesis. A considerably higher CPX degradation is achieved in the presence of NaCl than in Na2SO4 or Na3PO4 media due to the active chlorine generation. A faster CPX degradation is reached when the current density is increased or the pH value is lowered. This last behavior may be ascribed to an acid-catalyzed reaction between HClO and CPX. Degradation rates of 22.5, 3.96, and 0.576 mu mol L-1 min(-1) were observed for DW, MWW and urine, respectively. The lower efficiency measured in these last two effluents was related to the presence of organic matter and urea in the matrix. A degradation pathway is proposed based on HPLC-DAD and HPLC-MS analysis, indicating the fast formation (5 min) of CPX-(S)-sulfoxide and CPX-(R)-sull'oxide, generated due the Cl-2-active attack at the CPX thioether. Furthermore, antimicrobial activity elimination of the treated solution is reached once CPX, and the initial by-products are considerably eliminated. Finally, even if only 16% of initial TOC is removed, BOD5 tests prove the ability of electro-generated Cl-2-active to transform the antibiotic into biodegradable compounds. A similar strategy can be used for the abatement of other recalcitrant compounds contained in real water matrices such as urine and municipal wastewaters. Published by Elsevier B.V.
机译:在不同的流出物中评估在Ti / Ruo2-IRO2阳极上使用电生产生的Cl-2活性消除Cephalexin(CPX):去离子水(DW),城市废水(MWW)和尿液。制备单Ti / RuO2和Ti / IRO2催化剂以比较它们的形态和电化学行为对二元DSA。 XRD和外形细化表明Ti / RuO2-IRO2形成固溶体,其中Ru2和Iro(2)生长通过Ru原子取代其金红石型结构。 SCM揭示了所有催化剂的平坦区域的泥裂结构,而EDS分析表明在合成期间使用的标称浓度的氧化物化学物质系列中的原子比。由于活性氯产生,在NaCl存在下,在NaCl存在下实现显着更高的CPX降解。当电流密度增加或降低pH值时,达到更快的CPX劣化。该最后行为可以归因于HCLO和CPX之间的酸催化反应。为DW,MWW和尿液分别观察到22.5,3.96和0.576μmL-1分钟(-1)的降解速率。在这些最后两种流出物中测量的较低效率与基质中有机物和尿素的存在有关。基于HPLC-DAD和HPLC-MS分析提出了降解途径,表明CPX-(S) - 硫氧化物的快速形成(5分钟)和CPX-(R)-Sull' -Ullide,产生的CL-2-积极攻击CPX硫醚。此外,一旦CPX达到了抗微生物活性消除处理的溶液,并且显着消除了初始副产物。最后,即使仅移除了16%的初始TOC,BOD5测试也证明了电生产生的CL-2活性能力将抗生素转化为可生物降解的化合物。类似的策略可用于削减实际水基质中包含的其他核核糖化合物,例如尿和市政废水。由elsevier b.v出版。

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