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首页> 外文期刊>Journal of Hazardous Materials >Degradation of trans-ferulic acid in acidic aqueous medium by anodic oxidation, electro-Fenton and photoelectro-Fenton
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Degradation of trans-ferulic acid in acidic aqueous medium by anodic oxidation, electro-Fenton and photoelectro-Fenton

机译:阳极氧化,电芬顿和光电芬顿降解酸性水介质中的反式阿魏酸

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摘要

Solutions of pH 3.0 containing trans-ferulic acid, a phenolic compound in olive oil mill wastewater, have been comparatively degraded by anodic oxidation with electrogenerated H2O2 (AO-H2O2), electro-Fenton (EF) and photoelectro-Fenton (PEF). Trials were performed with a BDD/air-diffusion cell, where oxidizing (OH)-O-center dot was produced from water discharge at the BDD anode and/or in the solution bulk from Fenton's reaction between cathodically generated H2O2 and added catalytic Fe2+. The substrate was very slowly removed by AO-H2O2, whereas it was very rapidly, abated by EF and PEF, at similar rate in both cases, due to its fast reaction with (OH)-O-center dot in the bulk. The AO-H2O2 process yielded a slightly lower mineralization than EF, which promoted the accumulation of barely oxidizable products like Fe(III) complexes. In contrast, the fast photolysis of these latter species under irradiation with UVA light in PEF led to an almost total mineralization with 98% total organic carbon decay. The effect of current density and substrate concentration on the performance of all treatments was examined. Several solar PEF (SPEF) trials showed its viability for the treatment of wastewater containing trans-ferulic add at larger scale. Four primary aromatic products were identified by GC-MS analysis of electrolyzed solutions, and final carboxylic acids like fumaric, acetic and oxalic were detected by ion-exclusion HPLC. A reaction sequence for trans-ferulic acid mineralization involving all the detected products is finally proposed. (C) 2015 Elsevier B.V. All rights reserved.
机译:橄榄油厂废水中含有一种反式阿魏酸(一种酚类化合物)的pH 3.0溶液已通过用电生成的H2O2(AO-H2O2),电Fenton(EF)和光电Fenton(PEF)进行阳极氧化而相对降解。使用BDD /空气扩散池进行了试验,其中BDD阳极处的水排放和/或Fenton在阴极生成的H2O2和添加的催化Fe2 +之间的反应产生的大量溶液中产生了氧化(OH)-O-中心点。基材被AO-H2O2去除的速度非常慢,而被EF和PEF去除的速度非常快,在两种情况下,由于其与本体中的(OH)-O-中心点的快速反应,它们的去除速率相似。 AO-H2O2工艺产生的矿化度比EF略低,这促进了像Fe(III)配合物这样的几乎不可氧化的产物的积累。相反,在PEF中用UVA光照射后,这些后一种物质的快速光解导致几乎全部矿化,总有机碳衰减98%。检查了电流密度和底物浓度对所有处理性能的影响。几项太阳能PEF(SPEF)试验表明,该方法可大规模处理含反铁添加剂的废水。通过电解溶液的GC-MS分析确定了四种主要的芳族产物,并通过离子排阻HPLC检测了最终的羧酸,如富马酸,乙酸和草酸。最后提出了涉及所有检测到的产物的反式阿魏酸矿化的反应顺序。 (C)2015 Elsevier B.V.保留所有权利。

著录项

  • 来源
    《Journal of Hazardous Materials》 |2016年第5期|3-12|共10页
  • 作者单位

    Univ Barcelona, Fac Quim, Dept Quim Fis, Lab Electroquim Mat & Medi Ambient, Marti & Franques 1-11, E-08028 Barcelona, Spain;

    Univ Barcelona, Fac Quim, Dept Quim Fis, Lab Electroquim Mat & Medi Ambient, Marti & Franques 1-11, E-08028 Barcelona, Spain;

    Univ Barcelona, Fac Quim, Dept Quim Fis, Lab Electroquim Mat & Medi Ambient, Marti & Franques 1-11, E-08028 Barcelona, Spain;

    Univ Barcelona, Fac Quim, Dept Quim Fis, Lab Electroquim Mat & Medi Ambient, Marti & Franques 1-11, E-08028 Barcelona, Spain;

    Univ Barcelona, Fac Quim, Dept Quim Fis, Lab Electroquim Mat & Medi Ambient, Marti & Franques 1-11, E-08028 Barcelona, Spain;

    Univ Barcelona, Fac Quim, Dept Quim Fis, Lab Electroquim Mat & Medi Ambient, Marti & Franques 1-11, E-08028 Barcelona, Spain;

    Univ Barcelona, Fac Quim, Dept Quim Fis, Lab Electroquim Mat & Medi Ambient, Marti & Franques 1-11, E-08028 Barcelona, Spain;

  • 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);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Anodic oxidation; Electro-Fenton; Oxidation products; Photoelectro-Fenton trans-Ferulic acid;

    机译:阳极氧化;电子芬顿;氧化产物;光电芬顿反式果酸;

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