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The Application of an Activated Carbon Supported Cu-Ce/Ac Oxide Anode on the Electrocatalytic Degradation of Phenol

机译:活性炭负载的Cu-Ce / Ac氧化物阳极在苯酚电催化降解中的应用

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The Cu-AC (AC: activated carbon) and Cu/Ce-AC composite materials were synthesized using a one- pot sol-gel method. The surface microstructure and composition of the resulting samples were characterized by Brunauer–Emmett–Teller (BET) specific surface area analysis, scanning electron microscopy/energy dispersive x-ray(SEM/EDX), and XPS(X-ray photoelectron spectroscopy) compared to pure AC. Finally, the electrochemical catalytic activity of the prepared materials for the oxidative degradation of phenol were contrastively studied. It was found that the Cu/Ce-AC catalyst had larger surface area, greater pHPZC value (pH value at the point of zero charge), stronger ability to chemisorb active oxygen, and more possible forms of higher oxides generated from chemisorbed hydroxyl radicals, than AC and Cu/AC. These factors synthetically resulted in its more prominence electro catalytic activity for phenol degradation compared to AC and Cu/AC. The 50min continuous electrochemical degradation for phenol by using Cu/Ce-AC achieved over 97% COD and 80% TOC removals at initiate phenol concentration =504mg/L, temperature = 25℃, pH = 3.0 and j = 80 A·m-2. The considerable electro catalytic performance of Cu-Ce/AC material makes it a promising anode for electrochemical treatment of organic pollutants in aqueous solution.
机译:使用一锅溶胶-凝胶法合成了Cu-AC(活性炭)和Cu / Ce-AC复合材料。通过比较Brunauer-Emmett-Teller(BET)比表面积分析,扫描电子显微镜/能量色散X射线(SEM / EDX)和XPS(X射线光电子能谱)表征了所得样品的表面微观结构和组成。到纯交流电。最后,对比研究了所制备材料对苯酚氧化降解的电化学催化活性。发现Cu / Ce-AC催化剂具有更大的表面积,更大的pHPZC值(零电荷点的pH值),更强的化学吸附活性氧能力以及更多可能的形式是由化学吸附的羟基自由基生成,比AC和Cu / AC。这些因素综合导致与AC和Cu / AC相比,它对苯酚降解的电催化活性更高。在初始苯酚浓度= 504mg / L,温度= 25℃,pH = 3.0和j = 80 A·m-2的条件下,使用Cu / Ce-AC连续50min进行苯酚的电化学降解可实现超过97%的COD和80%的TOC去除率。 Cu-Ce / AC材料的出色的电催化性能使其成为用于电化学处理水溶液中有机污染物的有希望的阳极。

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