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首页> 外文期刊>Electrochimica Acta >Application of electrochemical advanced oxidation processes with a boron-doped diamond anode to degrade acidic solutions of Reactive Blue 15 (Turqueoise Blue) dye
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Application of electrochemical advanced oxidation processes with a boron-doped diamond anode to degrade acidic solutions of Reactive Blue 15 (Turqueoise Blue) dye

机译:掺硼金刚石阳极电化学高级氧化工艺在降解活性蓝15(Turqueoise Blue)染料的酸性溶液中的应用

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The degradation of the copper-phthalocyanine dye Reactive Blue 15 dye in sulfate medium has been comparatively studied by electrochemical oxidation with electrogenerated H2O2 (EO-H2O2), electro-Fenton (EF) and photoelectro-Fenton (PEF). Experiments with 100 cm(3) solutions of 0.203 mmol dm(-3) dye were performed with a stirred tank reactor containing a boron-doped diamond (BDD) anode and an air-diffusion cathode for continuous H2O2 production. Experimental conditions of pH 3.0 and 0.50 mmol dm(-3) Fe2+ as catalyst were found optimal for the EF process by the predominant oxidation with hydroxyl radicals formed in the bulk from Fenton's reaction between added Fe2+ and generated H2O2. The kinetics of Reactive Blue 15 abatement was followed by reversed-phase HPLC and always obeyed a pseudo-first-order reaction. The decolorization rate in EO-H2O2 was much lower than dye decay due to the formation of large quantities of colored intermediates under the action of hydroxyl radicals generated at the BDD anode from water oxidation. In contrast, the color and dye removals were much more rapid in EF and PEF by the most efficient oxidation of hydroxyl radicals produced from Fenton's reaction. PEF was the most powerful treatment owing to the photolytic action of UVA irradiation, yielding 94% mineralization after 360 min at 66.7 mA cm(-2). The effect of current density over the performance of all methods was examined. LC-MS analysis of treated solutions allowed the identification of 25 aromatic and heteroaromatic products and 30 hydroxylated derivatives. Tartaric, acetic, oxalic and oxamic acids were quantified by ion-exclusion HPLC. Acetic acid was the only product remaining after PEF and its large persistence explained the almost total mineralization achieved by this process. Chloride, sulfate, nitrate and in smaller proportion, ammonium ions were released to the solution in all cases. A plausible reaction sequence for Reactive Blue 15 mineralization has been finally proposed. (C) 2015 Elsevier Ltd. All rights reserved.
机译:通过用电生成的H2O2(EO-H2O2),电Fenton(EF)和光电Fenton(PEF)进行电化学氧化,比较研究了铜-酞菁染料活性蓝15染料在硫酸盐介质中的降解。使用带有0.23 mmol dm(-3)染料的100 cm(3)溶液的实验在搅拌釜反应器中进行,该反应器包含硼掺杂的金刚石(BDD)阳极和空气扩散阴极,用于连续生产H2O2。发现pH为3.0和0.50 mmol dm(-3)Fe2 +作为催化剂的实验条件最适合于EF工艺,主要是通过添加的Fe2 +与生成的H2O2之间的芬顿反应,在主体中形成大量的羟基自由基。反相HPLC追踪活性蓝15消减的动力学,并始终遵循拟一级反应。 EO-H2O2中的脱色率比染料衰减要低得多,这是由于在BDD阳极由水氧化产生的羟基自由基的作用下形成了大量有色的中间体而形成的。相比之下,通过芬顿反应产生的最有效的羟基氧化作用,EF和PEF中的颜色和染料去除要快得多。 PEF是最强大的处理方法,这是由于UVA辐射的光解作用,在66.7 mA cm(-2)下360分钟后产生94%的矿化作用。检查了电流密度对所有方法性能的影响。对处理过的溶液进行LC-MS分析后,可以鉴定出25种芳族和杂芳族产物以及30种羟基化衍生物。通过离子排斥HPLC对酒石酸,乙酸,草酸和草酰胺酸进行定量。乙酸是PEF之后唯一剩下的产品,其持久性高,说明了该工艺几乎实现了全部矿化作用。在所有情况下,氯离子,硫酸根,硝酸根以及较小比例的铵离子都会释放到溶液中。最终提出了活性蓝15矿化的合理反应顺序。 (C)2015 Elsevier Ltd.保留所有权利。

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