Dbira Sondos, Bensalah Nasr, Ahmad Mohammad I, Bedoui Ahmed
Department of Chemistry, Faculty of Sciences of Gabes, University of Gabes, 6072 Gabes, Tunisia.
Department of Chemistry and Earth Sciences, College of Arts and Science, Qatar University, P.O. Box 2713, Doha, Qatar.
Materials (Basel). 2019 Apr 16;12(8):1254. doi: 10.3390/ma12081254.
In the present work, electrochemical technology was used simultaneously for the deactivation of microorganisms and the destruction of micro-pollutants contained in synthetic urine wastewaters. Microorganisms () were added to synthetic urine wastewaters to mimic secondary treated sewage wastewaters. Different anode materials were employed including boron-doped diamond (BDD), dimensionally stable anode (DSA: IrO and RuO) and platinum (Pt). The results showed that for the different anode materials, a complete deactivation of microorganisms at low applied electric charge (1.34 Ah dm) was obtained. The complete deactivation of microorganisms in wastewater seems to be directly related to active chlorine and oxygen species electrochemically produced at the surface of the anode material. Complete depletion of COD and TOC can be attained during electrolyses with BDD anode after the consumption of specific electric charges of 4.0 and 8.0 Ah dm, respectively. Higher specific electric charges (>25 Ah dm) were consumed to removal completely COD and about 75% of TOC during electrolyses with DSA anodes (IrO and RuO). However, the electrolysis using Pt anode can partially remove and even after the consumption of high specific electric charges (>40 Ah dm) COD and TOC did not exceed 50 and 25%, respectively. Active chlorine species including hypochlorite ions and chloramines formed during electrolysis contribute not only to deactivate microorganisms but also to degrade organics compounds. High conversion yields of organic nitrogen into nitrates and ammonium were achieved during electrolysis BDD and DSA anodes. The results have confirmed that BDD anode is more efficient than with IrO, RuO and Pt electrodes in terms of COD and TOC removals. However, higher amounts of perchlorates were measured at the end of the electrolysis using BDD anode.
在本研究中,电化学技术被同时用于使微生物失活以及破坏合成尿液废水中所含的微量污染物。向合成尿液废水中添加微生物()以模拟二级处理后的污水废水。采用了不同的阳极材料,包括硼掺杂金刚石(BDD)、尺寸稳定阳极(DSA:IrO 和 RuO)以及铂(Pt)。结果表明,对于不同的阳极材料,在低施加电荷(1.34 Ah dm)时微生物可实现完全失活。废水中微生物的完全失活似乎与在阳极材料表面电化学产生的活性氯和氧物种直接相关。使用BDD阳极进行电解时,分别消耗4.0和8.0 Ah dm的特定电荷后,可实现COD和TOC的完全去除。使用DSA阳极(IrO和RuO)进行电解时,需要消耗更高的特定电荷(>25 Ah dm)才能完全去除COD和约75%的TOC。然而,使用Pt阳极进行电解只能部分去除,即使消耗了高特定电荷(>40 Ah dm),COD和TOC分别也不超过50%和25%。电解过程中形成的包括次氯酸根离子和氯胺在内的活性氯物种不仅有助于使微生物失活,还能降解有机化合物。在BDD和DSA阳极电解过程中,有机氮向硝酸盐和铵的转化率很高。结果证实,在COD和TOC去除方面,BDD阳极比IrO、RuO和Pt电极更高效。然而,使用BDD阳极进行电解结束时,测得的高氯酸盐含量更高。