No abstract

Electro-catalytic technology has attracted increasing attention as a promising approach for wastewater treatment, owing to its easy operation, minimal generation of secondary pollution, small foot-print and rapid start-up. In this work, the chlorine evolution potential of the Pd-Sn modi ed ruthenium(Ru)iridium(Ir) electrode was investigated for electro-catalytic treatment of high chlorine ammonia-nitrogen wastewater. The effect of reaction conditions on the removal of ammonia-nitrogen, kinetics and apparent activation energy of the electro-catalytic treatment of ammonia-nitrogen were studied. The possible denitri cation process of high chlorine ammonia-nitrogen wastewater treated by electrocatalysis was discussed. The results indicated that the chlorine evolution potential of the Pd-Sn modi ed Ru-Ir electrode was 1.0956 V(vs. SCE). The rule of electro-catalytic treatment of high chlorine ammonia-nitrogen conformed to zero-order kinetics, and the removal process was endothermic reaction with the apparent activation energy of 14.089 kJ/mol. With the current is 0.5 A, the removal e ciency of ammonia-nitrogen could achieve 100% at the reaction time of 40 min. Indirect oxidation played an essential role in the electro-catalytic ammonia-nitrogen removal using the Pd-Sn modi ed Ru-Ir electrode. This paper demonstrated that the electro-catalytic technology was a promising approach for e ciently treating the high chlorine ammonia-nitrogen wastewater.

No abstract

Electro-catalytic technology has attracted increasing attention as a promising approach for wastewater treatment, owing to its easy operation, minimal generation of secondary pollution, small foot-print and rapid start-up. In this work, the chlorine evolution potential of the Pd-Sn modified ruthenium(Ru)-iridium(Ir) electrode was investigated for electro-catalytic treatment of high chlorine ammonia-nitrogen wastewater. The effect of reaction conditions on the removal of ammonia-nitrogen, kinetics and apparent activation energy of the electro-catalytic treatment of ammonia-nitrogen were studied. The possible denitrification process of high chlorine ammonia-nitrogen wastewater treated by electrocatalysis was discussed. The results indicated that the chlorine evolution potential of the Pd-Sn modified Ru-Ir electrode was 1.0956 V(vs. SCE). The rule of electro-catalytic treatment of high chlorine ammonia-nitrogen conformed to zero-order kinetics, and the removal process was endothermic reaction with the apparent activation energy of 14.089 kJ/mol. With the current is 0.5 A, the removal efficiency of ammonia-nitrogen could achieve 100% at the reaction time of 40 min. Indirect oxidation played an essential role in the electro-catalytic ammonia-nitrogen removal using the Pd-Sn modified Ru-Ir electrode. This paper demonstrated that the electro-catalytic technology was a promising approach for efficiently treating the high chlorine ammonia-nitrogen wastewater.