State Key Laboratory of Pollution Control and Resources Reuse, School of Environment, Nanjing University, Jiangsu, Nanjing, 210023, PR China.
State Key Laboratory of Pollution Control and Resources Reuse, School of Environment, Nanjing University, Jiangsu, Nanjing, 210023, PR China.
Chemosphere. 2019 Apr;221:314-323. doi: 10.1016/j.chemosphere.2019.01.036. Epub 2019 Jan 8.
In the present work, we first examined the performance of zero-valent iron (Fe) activated peroxymonosulfate (PMS) for the removal of that bisphenol M (BPM). In 90 min, 95.9 ± 1.0% of BPM (initial concentration of 10 μM) could be removed in the optimal reaction conditions: [BPM]:[PMS] = 1:40 (molar ratio), [PMS]:[Fe] = 1:3 (molar ratio), pH = 8.0 (maintained by 0.1 M phosphate buffer solution), T = 35 °C. Common environmental ions like HCO, Cl, NO accelerated BPM degradation while NH hindered it. In radical quenching tests, sulfate radicals (SO) were found to play a dominant role in BPM degradation, while hydroxyl radicals (OH) were also detected. By high-performance liquid chromatography-tandem mass spectrometry analysis, 13 products of BPM including small molecules, oligomers and hydroxylated derivatives were identified, and five possible degradation pathways were then proposed. The predicted acute toxicity of the reaction products was reduced after BPM was treated by Fe/PMS. All these results prove that Fe/PMS is an efficient, convenient, and environmentally friendly treatment method for the removal of BPM.
在本工作中,我们首先考察了零价铁(Fe)活化过一硫酸盐(PMS)去除双酚 M(BPM)的性能。在最佳反应条件下([BPM]:[PMS] = 1:40(摩尔比),[PMS]:[Fe] = 1:3(摩尔比),pH = 8.0(由 0.1 M 磷酸盐缓冲溶液维持),T = 35°C),90 min 内可去除 95.9 ± 1.0%的 BPM(初始浓度为 10 μM)。HCO、Cl、NO 等常见环境离子加速了 BPM 的降解,而 NH 则阻碍了其降解。在自由基猝灭实验中,发现硫酸根自由基(SO)在 BPM 降解中起主导作用,同时也检测到了羟基自由基(OH)。通过高效液相色谱-串联质谱分析,鉴定出 BPM 的 13 种产物,包括小分子、低聚物和羟化衍生物,随后提出了 5 种可能的降解途径。Fe/PMS 处理后,反应产物的预测急性毒性降低。所有这些结果都证明了 Fe/PMS 是一种高效、方便、环保的去除 BPM 的处理方法。