Wu Juan-li, Zhang Jia-wei, Wang Ting, Ni Jin-ren
Huan Jing Ke Xue. 2015 Jul;36(7):2540-6.
Electrochemical systems were built to investigate the degradation of benzotriazole (BTA) on boron-doped diamond (BUU) and PbO2 anodes and give an insight into the mineralization ability of two electrodes in terms of the amount and activity of hydroxyl radicals. Results of bulk electrolysis showed that both BDD and PbO2 displayed perfect BTA degradation performance after 12 hours' electrolysis, with the removal percentages of 99. 48% and 98. 36%, respectively, while the mineralization ability of BDD was much stronger than that of PbO2, with the efficiency of 87. 69% for BDD and 35. 96% for PbO2. Less hydroxyl radical and hydrogen production in BDD system suggested the less amount of active sites on BDD surface, thus further verified that the generated hydroxyl radical amount was not the primary factor determining the mineralization ability of anodes. However, BDD displayed larger binding energy of adsorbed oxygen and thinner adsorption layer than those of PbO2, indicating that the BDD electrode surface was of greater catalytic activity, thus the generated hydroxyl radicals were more free, which was the key to its better mineralization ability.
构建了电化学系统,以研究硼掺杂金刚石(BDD)和PbO₂阳极上苯并三唑(BTA)的降解情况,并根据羟基自由基的数量和活性深入了解两种电极的矿化能力。批量电解结果表明,BDD和PbO₂在电解12小时后均表现出优异的BTA降解性能,去除率分别为99.48%和98.36%,而BDD的矿化能力远强于PbO₂,BDD的效率为87.69%,PbO₂为35.96%。BDD体系中羟基自由基和氢气产量较少,表明BDD表面活性位点数量较少,从而进一步证实,产生的羟基自由基数量不是决定阳极矿化能力的主要因素。然而,BDD比PbO₂表现出更大的吸附氧结合能和更薄的吸附层,这表明BDD电极表面具有更高的催化活性,因此产生的羟基自由基更自由,这是其具有更好矿化能力的关键。