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Mechanism of electrochemical evolution of chlorine and oxygen at Ti/SnO2-IrO2 anode
作者姓名:Zhuo  CAI
作者单位:1. Faculty of Applied Sciences, University of the West of England, Coldharbour Lane, Bristol, BS16 1QY, UK; 2. Faculty of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, China
摘    要:The mechanisms of chlorine and oxygen electrochemical evolution at a novel Ti/SnO2-IrO2 anode were investigated using cyclic voltammetry and steady state current?potential measurements. For this study a laboratory constructed model cell was employed. Firstly, controlled potential electrolysis of 0.1 mol/L NaCl was performed and chlorine was observed to evolve at potential +1.2 V. The pH values of the solution decreased during electrolysis over the potential range of +1.0 V?+2.0 V, suggesting that oxygen evolution may involve in the reactions. Electrolysis with a de?oxygenated NaCl solution at a fixed potential of +2.0 V confirmed that O2 is one of the products generated at the anode. Further electrolysis of NaCl solution was conducted under steady state conditions. A potential?current density plot was constructed over the potential range of +1.00 V?+1.28 V. The slope of the plot at Tafel section was found to be 41 mV/decade. These results indicate that chlorine evolution at the anode is achieved via an intermediate layer formed by electrosorption of oxygen and chlorine on the electrode surface.

关 键 词:NaCl    electrode  reactions    chlorine  evolution    oxygen  evolution.

Mechanism of electrochemical evolution of chlorine and oxygen at Ti/SnO2-IrO2 anode
Zhuo CAI.Mechanism of electrochemical evolution of chlorine and oxygen at Ti/SnO2-IrO2 anode[J].Progress in Natural Science,2005,15(13):76-81.
Authors:Zhuo CAI
Abstract:The mechanisms of chlorine and oxygen electrochemical evolution at a novel Ti/SnO2-IrO2 anode were investigated using cyclic voltammetry and steady state current?potential measurements. For this study a laboratory constructed model cell was employed. Firstly, controlled potential electrolysis of 0.1 mol/L NaCl was performed and chlorine was observed to evolve at potential +1.2 V. The pH values of the solution decreased during electrolysis over the potential range of +1.0 V?+2.0 V, suggesting that oxygen evolution may involve in the reactions. Electrolysis with a de?oxygenated NaCl solution at a fixed potential of +2.0 V confirmed that O2 is one of the products generated at the anode. Further electrolysis of NaCl solution was conducted under steady state conditions. A potential?current density plot was constructed over the potential range of +1.00 V?+1.28 V. The slope of the plot at Tafel section was found to be 41 mV/decade. These results indicate that chlorine evolution at the anode is achieved via an intermediate layer formed by electrosorption of oxygen and chlorine on the electrode surface.
Keywords:NaCl  electrode reactions  chlorine evolution  oxygen evolution  
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