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Combination with catalyzed Fe(0)-carbon microelectrolysis and activated carbon adsorption for advanced reclaimed water treatment: simultaneous nitrate and biorefractory organics removal

机译:<粗体>与催化Fe(0)的组合 - 用于高级再生水处理的碳微电子和活性炭吸附:同时硝酸盐和生物用具有机物去除

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摘要

A process combining catalyzed Fe(0)-carbon microelectrolysis (IC-ME) with activated carbon (AC) adsorption was developed for advanced reclaimed water treatment. Simultaneous nitrate reduction and chemical oxygen demand (COD) removal were achieved, and the effects of composite catalyst (CC) addition, AC addition, and initial pH were investigated. The reaction kinetics and reaction mechanisms were calculated and analyzed. The results showed that CC addition could enhance the reduction rate of nitrate and effectively inhibit the production of ammonia. Moreover, AC addition increased the adsorption capacity of biorefractory organic compounds (BROs) and enhanced the degradation of BRO. The reduction of NO3--N at different pH values was consistently greater than 96.9%, and NH4+-N was suppressed by high pH. The presence of CC ensured the reaction rate of IC-ME at high pH. The reaction kinetics orders and constants were calculated. Catalyzed iron scrap (IS)-AC showed much better nitrate reduction and BRO degradation performances than IS-AC and AC. The IC-ME showed great potential for application to nitrate and BRO reduction in reclaimed water.
机译:将催化的Fe(0) - 碳微电子(IC-ME)与活性炭(AC)吸附结合的方法进行了高级再生水处理。实现了同时硝酸盐还原和化学需氧量(COD)去除,并研究了复合催化剂(CC)添加,AC添加和初始pH的作用。计算并分析反应动力学和反应机制。结果表明,CC添加可以增强硝酸盐的还原率,有效地抑制氨的产生。此外,AC添加增加了生物氟色有机化合物(兄弟)的吸附能力,增强了兄弟的降解。在不同pH值下的NO 3-N的还原始终大于96.9%,高pH抑制NH 4 + -N。 CC的存在确保了高pH的IC-ME反应速率。计算反应动力学订单和常数。催化的铁废料(IS)-Ac表现出比IS-AC和AC的更好的硝酸盐还原和稀释性降解性能。 IC-ME表现出应用于硝酸盐和再生水中的盐水的潜力。

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