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DOI 10.1016/j.jhazmat.2010.04.048

Медицинская библиотека · Journal of hazardous materials · 2010

Electrochemical oxidation of synthetic tannery wastewater in chloride-free aqueous media.

Costa Carla Regina, Montilla Francisco, Morallón Emilia, Olivi Paulo

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

The electrochemical treatment of a synthetic tannery wastewater, prepared with several compounds used by finishing tanneries, was studied in chloride-free media. Boron-doped diamond (Si/BDD), antimony-doped tin dioxide (Ti/SnO(2)-Sb), and iridium-antimony-doped tin dioxide (Ti/SnO(2)-Sb-Ir) were evaluated as anode. The influence of pH and current density on the treatment was assessed by means of the parameters used to measure the level of organic contaminants in the wastewater; i.e., total phenols, chemical oxygen demand (COD), total organic carbon (TOC), and absorbance. Results showed that faster decrease in these parameters occurred when the Si/BDD anode was used. Good results were obtained with the Ti/SnO(2)-Sb anode, but its complete deactivation was reached after 4h of electrolysis at 25 mA cm(-2), indicating that the service life of this electrode is short. The Ti/SnO(2)-Sb-Ir anode is chemically and electrochemically more stable than the Ti/SnO(2)-Sb anode, but it is not suitable for the electrochemical treatment under the studied conditions. No significant changes were observed for electrolyses performed at different pH conditions with Si/BDD, and this electrode led to almost complete mineralization after 4h of electrolysis at 100 mA cm(-2). The increase in current density resulted in faster wastewater oxidation, with lower current efficiency and higher energy consumption. Si/BBD proved to be the best electrodic material for the direct electrooxidation of tannery wastewaters.

Для цитирования: Costa Carla Regina, Montilla Francisco, Morallón Emilia, Olivi Paulo. Electrochemical oxidation of synthetic tannery wastewater in chloride-free aqueous media.. Journal of hazardous materials. 2010. DOI: 10.1016/j.jhazmat.2010.04.048.

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