College of Architecture and Environment, Sichuan University, Chengdu 610065, China.
College of Architecture and Environment, Sichuan University, Chengdu 610065, China; National Engineering Laboratory for Clean Technology of Leather Manufacture, Sichuan University, Chengdu 610065, China.
Water Res. 2017 Apr 15;113:80-88. doi: 10.1016/j.watres.2017.02.016. Epub 2017 Feb 8.
The reaction between persulfate (PS) and carbon nanotubes (CNTs) for the degradation of 2,4-dichlorophenol (2,4-DCP) was investigated. It was demonstrated that CNTs could efficiently activate PS for the degradation of 2,4-DCP. Results suggested that the neither hydroxyl radical (OH) nor sulfate radical (SO) was produced therein. For the first time, the generation of singlet oxygen (O) was proved by several methods including electron paramagnetic resonance spectrometry (EPR) and liquid chromatography mass spectrometry measurements. Moreover, the generation of the superoxide radical as a precursor of the singlet oxygen was also confirmed by using certain scavengers and EPR measurement, in which the presence of molecular oxygen was not required as a precursor of O. The efficient generation of O using the PS/CNTs system without any light irradiation can be employed for the selective oxidation of aqueous organic compounds under neutral conditions with the mineralization and toxicity evaluated. A kinetic model was developed to theoretically evaluate the adsorption and oxidation of 2,4-DCP on the CNTs. Accordingly, a catalytic mechanism was proposed involving the formation of a dioxirane intermediate between PS and CNTs, and the subsequent decomposition of this intermediate into O.
过硫酸盐(PS)与碳纳米管(CNTs)之间的反应可用于降解 2,4-二氯苯酚(2,4-DCP)。结果表明,CNTs 可有效激活 PS 以降解 2,4-DCP。研究结果表明,其中既没有生成羟基自由基(OH),也没有生成硫酸根自由基(SO)。本文首次通过电子顺磁共振波谱(EPR)和液相色谱质谱联用等多种方法证明了单线态氧(O)的生成。此外,通过使用某些猝灭剂和 EPR 测量还证实了超氧自由基的生成,该自由基是单线态氧的前体,而 O 的前体不需要分子氧。在没有任何光照的情况下,使用 PS/CNTs 体系可以有效地生成 O,可用于在中性条件下选择性氧化水中的有机化合物,并对其矿化和毒性进行评估。本文建立了一个动力学模型,从理论上评估了 2,4-DCP 在 CNTs 上的吸附和氧化。因此,提出了一种涉及 PS 和 CNTs 之间形成二氧杂环戊烷中间体,以及随后该中间体分解为 O 的催化机制。