碱性溶液中硼氢化钠在铜阳极上的氧化行为

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Polarization data of BH_4~- oxidation on Cu anode in alkaline solution were measured at steady state by a self-made experimental cell. The experimental polarization curve showed three regions: the region at lower over-potential η (below 0. 4 V approximately), the region at higher η (above 0. 6 V approximately) and the transitional region at medium η. It was found that the limiting current density is caused by the limiting elemental step rather than the external mass transport. The apparent reaction order with respect to BH_4~- changes from 0 to 1. The active energy is about 40 kJ·mol~(-1) in both regions with lower and higher η, and is higher than 40 kJ· mol~(-1) in the transitional region. With the experimental temperatures and NaOH concentration, the hydrogen production rates released by the electrode reaction were measured at [BH_4~- ] /[OH~-] ratios of 1: 40, 1: 20, 1: 6. 7 and 1:4, which is strongly dependent on the over-potential. The apparent number of released electron n by the reaction was calculated by using the measured amounts of hydrogen and coulomb. Higher value of n was obtained at lower [BH_4~1 ] /[OH~- ] ratio, higher temperature as well as higher over-potential. Under the experimental conditions, the value of n varies from 0 to 7, while in the transitional region it is just in the range of 3 to 5. The experimental results indicate that the limiting current density or n value will increase by virtue of proper experimental conditions. However, to considerably increase the current density at lower over-potential requires a modified anode with higher activity.
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