Wang Lei, Jiang Xuanzhen, Liu Yongjun
Department of Chemistry, Zhejiang University, Hangzhou 310027, PR China.
J Hazard Mater. 2008 Jun 15;154(1-3):1106-14. doi: 10.1016/j.jhazmat.2007.11.016. Epub 2007 Nov 17.
Degradation of bisphenol A (BPA) and simultaneous formation of hydrogen peroxide induced by glow discharge plasma in contact with aqueous solution were investigated. Experimental results indicated that the BPA degradation rate was higher in sodium chloride solution than that in sodium sulfate or phosphate solutions. However, the formation rates of hydrogen peroxide were on the opposite case. Both the BPA removal and the hydrogen peroxide production rates decreased in the presence of hydroxyl radical scavengers, indicating that hydroxyl radicals are the most probable oxidants responsible for BPA degradation and the precursors of hydrogen peroxide. Ferric ion showed better catalytic effect than that of ferrous ion, suggesting that the ferric ion was reduced by the intermediates formed during BPA degradation, which was confirmed by following the production of ferrous ion in the system. TOC of the solution gradually reduced with discharge time; however, without catalysts, the solution COD increased with discharge time and sharply decreased in the presence of iron salts. The major intermediate products were identified by LC/MS and the possible degradation mechanism was discussed.
研究了辉光放电等离子体与水溶液接触时双酚A(BPA)的降解及同时产生过氧化氢的情况。实验结果表明,BPA在氯化钠溶液中的降解速率高于在硫酸钠或磷酸盐溶液中的降解速率。然而,过氧化氢的生成速率情况则相反。在存在羟基自由基清除剂的情况下,BPA的去除率和过氧化氢的生成率均降低,这表明羟基自由基是最有可能负责BPA降解的氧化剂以及过氧化氢的前体。铁离子显示出比亚铁离子更好的催化效果,这表明铁离子被BPA降解过程中形成的中间体还原,通过跟踪体系中亚铁离子的产生得以证实。溶液的总有机碳(TOC)随放电时间逐渐降低;然而,在没有催化剂的情况下,溶液的化学需氧量(COD)随放电时间增加,而在存在铁盐的情况下急剧下降。通过液相色谱/质谱联用(LC/MS)鉴定了主要的中间产物,并讨论了可能的降解机制。