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首页> 外文期刊>Chemosphere >Effective mineralization of quinoline and bio-treated coking wastewater by catalytic ozonation using CuFe_2O_4/Sepiolite catalyst: Efficiency and mechanism
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Effective mineralization of quinoline and bio-treated coking wastewater by catalytic ozonation using CuFe_2O_4/Sepiolite catalyst: Efficiency and mechanism

机译:使用Cufe_2O_4 / Sepiolite催化剂通过催化臭氧处理喹啉和生物处理焦化废水的有效矿化:效率和机理

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摘要

In this study, CuFe2O4 nanocomposite loaded on natural sepiolite (CuFe2O4/SEP) was prepared by the citrate sol-gel method. CuFe2O4/SEP was characterized by X-ray diffraction, Brunauer-Emmett-Teller adsorption analysis, scanning electron microscopy, and energy dispersive spectroscopy. The CuFe2O4/SEP composite was stable and showed an excellent catalytic activity for ozonation. The efficiency of quinoline mineralization in the catalytic ozonation with CuFe2O4/SEP was 90.3%, and this value was 5.4 times higher than that of the uncatalyzed ozonation (16.8%). The quinoline mineralization followed a pseudo first-order kinetics with all the catalysts. The rate constant for the mineralization of quinoline by ozonation in the presence of CuFe2O4/SEP was 0.0885 min(-1), which was 16.7 times higher than that in ozone alone (0.0053 min(-1) ). Radical scavenging tests revealed that hydroxyl radical (center dot OH) and superoxide radical (center dot O-2(-)) were the reactive oxygen species (ROS) in the quinoline degradation. In the presence of CuFe2O4/SEP, ozone and hydrogen peroxide were rapidly converted into the ROS. Although neutral and alkaline pH were more beneficial for the quinoline mineralization, CuFe2O4/SEP exhibited significant catalytic activity even under acidic conditions. Meanwhile, five-cycle successive tests suggested that CuFe2O4/SEP was recyclable and hence, stable. Furthermore, the feasibility of the catalytic ozonation for the treatment of biologically treated coking wastewater was evaluated. The catalytic ozonation resulted in 57.81% total organic carbon removal efficiency at 60 min, which was 2.9 times higher than that in the uncatalyzed ozonation (19.99%). (C) 2019 Elsevier Ltd. All rights reserved.
机译:在该研究中,通过柠檬酸溶胶 - 凝胶法制制备负载在天然海泡石(CUFE2O4 / SEP)上的CuFe2O4纳米复合材料。 CuFe2O4 / SEP的特征在于X射线衍射,Brunauer-Emmett-excersaItsion分析,扫描电子显微镜和能量分散光谱。 CuFe2O4 / SeP复合材料稳定,并显示出臭氧化的优异催化活性。用CUF2O4 / SEP催化臭氧化喹啉矿化的效率为90.3%,该值比未催化的臭氧化(16.8%)高5.4倍。喹啉矿化随后用所有催化剂进行伪首次动力学。在CUF2O4 / SEP存在下通过臭氧化喹啉矿化的速率常数为0.0885 min(-1),比单独的臭氧(0.0053min(-1))高16.7倍。激进的清除试验显示羟基自由基(中心点OH)和超氧化物自由基(中心点O-2( - ))是喹啉降解中的反应性氧物质(ROS)。在CuFe 2 O 4 / SEP的存在下,臭氧和过氧化氢迅速转化为ROS。虽然中性和碱性pH对喹啉矿化更有益,但即使在酸性条件下,CuFe2O4 / SEP也表现出显着的催化活性。同时,五周期的连续测试表明,CUFE2O4 / SEP可回收,因此稳定。此外,评价了用于治疗生物处理的焦化废水的催化臭氧化的可行性。催化臭氧化导致60分钟的总机碳除载效率为57.81%,比未催化的臭氧化(19.99%)高2.9倍。 (c)2019 Elsevier Ltd.保留所有权利。

著录项

  • 来源
    《Chemosphere 》 |2019年第7期| 647-656| 共10页
  • 作者单位

    China Univ Min & Technol Beijing Sch Chem & Environm Engn Beijing 100083 Peoples R China;

    China Univ Min & Technol Beijing Sch Chem & Environm Engn Beijing 100083 Peoples R China;

    China Univ Min & Technol Beijing Sch Chem & Environm Engn Beijing 100083 Peoples R China;

    China Univ Min & Technol Beijing Sch Chem & Environm Engn Beijing 100083 Peoples R China;

    China Univ Min & Technol Beijing Sch Chem & Environm Engn Beijing 100083 Peoples R China;

    China Univ Min & Technol Beijing Sch Chem & Environm Engn Beijing 100083 Peoples R China;

    China Univ Min & Technol Beijing Sch Chem & Environm Engn Beijing 100083 Peoples R China;

    China Univ Min & Technol Beijing Sch Chem & Environm Engn Beijing 100083 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《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    CuFe2O4/Sepiolite; Catalytic ozonation; Quinoline; Mechanism; Biologically treated coking wastewater;

    机译:Cufe2O4 /海硫酸盐;催化臭氧化;喹啉;机制;生物处理的焦化废水;

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