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Degradation of antibiotic ampicillin on boron-doped diamond anode using the combined electrochemical oxidation - Sodium persulfate process

机译:电化学氧化-过硫酸钠组合电化学降解硼掺杂金刚石阳极上的氨苄青霉素

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In this work, the electrochemical oxidation of antibiotic ampicillin (AMP) on a boron-doped diamond anode in the presence of sodium persulfate (SPS) was investigated (EO/SPS process). Experiments were conducted at AMP concentrations between 0.8 and 3 mg/L, SPS concentrations between 100 and 500 mg/L, current densities between 5 and 110 mA/cm(2), in three water matrices (ultrapure water, bottled water and secondary treated wastewater), using 0.1 M Na2SO4 as the supporting electrolyte. AMP degradation follows a pseudo-first order kinetic expression with the apparent rate constant increasing with (i) increasing SPS concentration (from 0.08 min(-1) to 0.36 min(-1) at 0 and 500 mg/L SPS, respectively, 1.1 mg/L AMP, 25 mA/cm(2)), (ii) increasing current (from 0.08 min(-1) to 0.6 min(-1) at 5 and 110 mA/cm(2), respectively, 1.1 mg/L AMP, 250 mg/L SPS), and (iii) decreasing AMP concentration (from 0.16 min(-1) to 0.31 min(-1) at 3 and 0.8 mg/L, respectively, 250 mg/L SPS, 25 mA/cm(2)). The presence of various anions (mainly bicarbonates) in bottled water did not impact AMP degradation. The observed kinetic constant decreased by 40% in the presence of 10 mg/L humic acid. On the other hand, process efficiency was enhanced almost 3.5 times in secondary effluent due to the electrogeneration of active chlorine species that promote indirect oxidation reactions in the bulk solution. The efficacy of the EO/SPS process was compared to and found to be considerably greater than a process where SPS was activated by simulated solar irradiation at an intensity of 7.3 x 10(-7) E/(L.s) (SLR/SPS process). Coupling the two processes (EO/SLR/SPS) resulted in a cumulative, in terms of AMP degradation, effect. The combined process was tested for AMP degradation, mineralization and inhibition to Vibrio fischeri in wastewater; fast AMP removal was accompanied by low mineralization and incomplete toxicity removal.
机译:在这项工作中,研究了在过硫酸钠(SPS)存在下在掺硼金刚石阳极上抗生素氨苄青霉素(AMP)的电化学氧化(EO / SPS工艺)。在三种水基质(超纯水,瓶装水和二次处理水)中,以AMP浓度为0.8至3 mg / L,SPS浓度为100至500 mg / L,电流密度为5至110 mA / cm(2)进行实验废水),使用0.1 M Na2SO4作为支持电解质。 AMP降解遵循伪一级动力学表达,其表观速率常数随(i)SPS浓度的增加而增加(在0和500 mg / L SPS时,分别从0.08 min(-1)到0.36 min(-1),1.1 mg / L AMP,25 mA / cm(2)),(ii)增加电流(在5和110 mA / cm(2)时分别从0.08 min(-1)到0.6 min(-1),1.1 mg / L L AMP,250 mg / L SPS),和(iii)降低AMP浓度(分别在3和0.8 mg / L时从0.16 min(-1)降至0.31 min(-1),250 mg / L SPS,25 mA / cm(2))。瓶装水中各种阴离子(主要是碳酸氢盐)的存在不会影响AMP的降解。在10 mg / L腐殖酸存在下,观察到的动力学常数降低了40%。另一方面,由于活性氯物质的电生成促进了本体溶液中的间接氧化反应,因此二级废水的处理效率提高了近3.5倍。与EO / SPS工艺的功效进行比较,发现它比通过模拟太阳辐射以7.3 x 10(-7)E /(Ls)的强度激活SPS的工艺(SLR / SPS工艺)要强得多。 。就AMP降解而言,两个过程(EO / SLR / SPS)的结合产生了累积效应。测试了该组合工艺对废水中AMP的降解,矿化和对费氏弧菌的抑制作用;快速AMP去除伴随着低矿化和不完全毒性去除。

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