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Ozonation of aqueous phenol catalyzed by biochar produced from sludge obtained in the treatment of coking wastewater

机译:在焦化废水处理中获得的污泥产生的生物炭催化的苯酚臭氧化

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摘要

Sludge collected from industrial wastewater treatment possesses a threatening effect on environment, and changing it into functional material provides an alternative for its disposal. Biochar synthesized by pyrolysis of sludge obtained from coking wastewater treatment was evaluated for the catalytic ozonation of phenol in aqueous solution. The present work focused on testing the catalytic performance of biochar, deducing the kinetics of phenol removal in various reaction conditions, and finally elucidating the mechanism of biochar-enhanced phenol removal. The results demonstrated that biochars produced at pyrolysis temperatures of 700 and 900 °C revealed highly comparable catalytic activity in phenol ozonation, leading to around 95% phenol removal within 30 min reaction, due to the abundant carbonyl groups on biochar surface. The biochar, however, was suffered from poor stability, which was attributed to biochar loss and changes in surface chemistry. On the basis of examining reaction variables, an empirical kinetic model was developed well matching experimental results. It was found that ozone concentration adsorbed on biochar surface was first increased with a peak (3.8 mg/L for biochar obtained at 700 °C) at reaction time 10 min, after which it decreased along with proceeding reaction. In light of radical scavenging test, superoxide radical (O2ˉ) was identified as main radical species produced from the interaction of ozone with biochar surface, while hydroxyl radical (OH) played negligible role in biochar catalytic ozonation. The promoting mechanism of bicarbonate on phenol ozonation was verified to be the generation of O2ˉ via series reactions of HCO3ˉ with OH and ozone, apart from increase in solution pH. These results provide important implications for future recycling of coking wastewater treatment sludge in environmental remediation.
机译:从工业废水处理中收集的污泥对环境具有威胁性,将其转变为功能性材料提供了另一种处理方法。评价了焦化废水处理后的污泥经热解合成的生物炭对水溶液中苯酚的催化臭氧氧化作用。目前的工作集中在测试生物炭的催化性能,推导在各种反应条件下脱除苯酚的动力学,并最终阐明生物炭增强的苯酚脱除的机理。结果表明,在700和900 C的热解温度下产生的生物炭在苯酚臭氧化反应中显示出高度可比的催化活性,由于生物炭表面上有大量的羰基,因此在30min的反应中苯酚的去除率约为95%。然而,生物炭的稳定性差,这归因于生物炭的损失和表面化学的变化。在检查反应变量的基础上,建立了与实验结果完全匹配的经验动力学模型。发现在反应时间10分钟,吸附在生物炭表面的臭氧浓度首先增加一个峰值(在700℃下获得的生物炭为3.8μmg/ L),然后随着进行的反应而降低。根据自由基清除试验,将超氧自由基(O2ˉ)鉴定为臭氧与生物炭表面相互作用产生的主要自由基,而羟基自由基(OH)在生物炭催化臭氧化中的作用可忽略不计。碳酸氢盐对苯酚臭氧化的促进机理被证实是除溶液pH值增加外,还通过HCO3 +与OH和臭氧的串联反应生成了O2 +。这些结果为今后在环境修复中回收焦化废水处理污泥提供了重要的启示。

著录项

  • 来源
    《Journal of Environmental Management》 |2018年第15期|376-386|共11页
  • 作者单位

    School of Environment and Energy, South China University of Technology;

    School of Environment and Energy, South China University of Technology;

    School of Environment and Energy, South China University of Technology;

    School of Environment and Energy, South China University of Technology;

    School of Environment and Energy, South China University of Technology,Department of Materials and Environmental Technology, Tallinn University of Technology;

    School of Biology and Biological Engineering, South China University of Technology;

    School of Environment and Energy, South China University of Technology;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Biochar; Kinetic modeling; Ozone adsorption; Superoxide radical; Inorganic anions;

    机译:生物炭;动力学建模;臭氧吸附;超氧自由基;无机阴离子;

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