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Degradation of Ofloxacin by Perylene Diimide Supramolecular Nanofiber Sunlight-Driven Photocatalysis

机译:ylene二酰亚胺超分子纳米纤维阳光驱动的光催化降解氧氟沙星

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摘要

This study describes a promising sunlight-driven photocatalyst for the treatment of ofloxacin and other fluoroquinolone antibiotics in water and wastewater. Perylene diimide (PDI) supramolecular nanofibers, which absorb a broad spectrum of sunlight, were prepared via a facile acidification polymerization protocol. Under natural sunlight, the PDI photocatalysts achieved rapid treatment of fluoroquinolone antibiotics, including ciprofloxacin, enrofloxacin, norfloxacin, and ofloxacin. The fastest degradation was observed for ofloxacin, which had a half-life of 2.08 min for the investigated conditions. Various light sources emitting in the UV-vis spectrum were tested, and blue light was found to exhibit the fastest ofloxacin transformation kinetics due to the strong absorption by the PDI catalyst. Reactive species, namely, h(+), O-1(2), and O-2(center dot-), comprised the primary photocatalytic mechanisms for ofloxacin degradation. Frontier electron density calculations and mass spectrometry were used to verify the major degradation pathways of ofloxacin by the PDI-sunlight photocatalytic system and identify the transformation products of ofloxacin, respectively. Degradation mainly occurred through demethylation at the piperazine ring, ketone formation at the morpholine moiety, and aldehyde reaction at the piperazinyl group. An overall mechanism was proposed for ofloxacin degradation in the PDI-sunlight photocatalytic system, and the effects of water quality constituents were examined to determine performance in real water/wastewater systems. Ultimately, the aggregate results from this study highlight the suitability of the PDI-sunlight photocatalytic system to treat antibiotics in real water and wastewater systems.
机译:这项研究描述了一种有前途的阳光驱动光催化剂,用于处理水和废水中的氧氟沙星和其他氟喹诺酮抗生素。 f二酰亚胺(PDI)的超分子纳米纤维吸收了宽广的阳光,是通过简便的酸化聚合方案制备的。在自然阳光下,PDI光催化剂可以快速处理氟喹诺酮类抗生素,包括环丙沙星,恩诺沙星,诺氟沙星和氧氟沙星。氧氟沙星的降解最快,在所研究的条件下半衰期为2.08分钟。测试了在UV-vis光谱中发射的各种光源,发现蓝光由于PDI催化剂的强吸收而显示出最快的氧氟沙星转化动力学。反应性物质,即h(+),O-1(2)和O-2(中心点),构成氧氟沙星降解的主要光催化机制。通过前沿电子密度计算和质谱法验证了PDI-阳光光催化系统对氧氟沙星的主要降解途径并鉴定了氧氟沙星的转化产物。降解主要通过在哌嗪环上的脱甲基,在吗啉部分上的酮形成以及在哌嗪基上的醛反应发生。提出了氧氟沙星在PDI-阳光光催化系统中降解的整体机理,并研究了水质成分的影响,以确定实际水/废水系统中的性能。最终,这项研究的总体结果突出了PDI-阳光光催化系统在实际供水和污水处理系统中处理抗生素的适用性。

著录项

  • 来源
    《Environmental Science & Technology》 |2019年第3期|1564-1575|共12页
  • 作者单位

    Tsinghua Univ, Beijing Key Lab Emerging Organ Contaminants Contr, State Key Joint Lab Environm Simulat & Pollut Con, Sch Environm, Beijing 100084, Peoples R China;

    Tsinghua Univ, Beijing Key Lab Emerging Organ Contaminants Contr, State Key Joint Lab Environm Simulat & Pollut Con, Sch Environm, Beijing 100084, Peoples R China|Univ Maryland Baltimore Cty, Dept Chem Biochem & Environm Engn, 1000 Hilltop Circle,Engn 314, Baltimore, MD 21250 USA;

    Tsinghua Univ, Beijing Key Lab Emerging Organ Contaminants Contr, State Key Joint Lab Environm Simulat & Pollut Con, Sch Environm, Beijing 100084, Peoples R China;

    Tsinghua Univ, Beijing Key Lab Emerging Organ Contaminants Contr, State Key Joint Lab Environm Simulat & Pollut Con, Sch Environm, Beijing 100084, Peoples R China;

    Tsinghua Univ, Beijing Key Lab Emerging Organ Contaminants Contr, State Key Joint Lab Environm Simulat & Pollut Con, Sch Environm, Beijing 100084, Peoples R China;

    Tsinghua Univ, Beijing Key Lab Emerging Organ Contaminants Contr, State Key Joint Lab Environm Simulat & Pollut Con, Sch Environm, Beijing 100084, Peoples R China;

    Tsinghua Univ, Beijing Key Lab Emerging Organ Contaminants Contr, State Key Joint Lab Environm Simulat & Pollut Con, Sch Environm, Beijing 100084, Peoples R China;

    Tsinghua Univ, Beijing Key Lab Emerging Organ Contaminants Contr, State Key Joint Lab Environm Simulat & Pollut Con, Sch Environm, Beijing 100084, Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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