Environ Sci Technol. 2015 Jan 20;49(2):1043-50. doi: 10.1021/es503741d.
We show that phenol can be effectively degraded by magnetite in the presence of persulfate (S2O8(2–)) under UVA irradiation. The process involves the radical SO4(–•), formed from S2O8(2–) in the presence of Fe(II). Although magnetite naturally contains Fe(II), the air-exposed oxide surface is fully oxidized to Fe(III) and irradiation is required to produce Fe(II). The magnetite + S2O8(2–) system was superior to the corresponding magnetite + H2O2 one in the presence of radical scavengers and in a natural water matrix, but it induced phenol mineralization in ultrapure water to a lesser extent. The leaching of Fe from the oxide surface was very limited, and much below the wastewater discharge limits. The reasonable performance of the magnetite/persulfate system in a natural water matrix and the low levels of dissolved Fe are potentially important for the removal of organic contaminants in wastewater.
我们表明,在 UVA 照射下,磁铁矿在过硫酸盐(S2O8(2–))存在的情况下可以有效地降解苯酚。该过程涉及自由基 SO4(–•),其由 S2O8(2–)在 Fe(II)存在下形成。尽管磁铁矿天然含有 Fe(II),但暴露于空气中的氧化物表面完全被氧化为 Fe(III),需要辐照才能产生 Fe(II)。在有自由基清除剂和天然水基质存在的情况下,磁铁矿+S2O8(2–)体系优于相应的磁铁矿+H2O2 体系,但在超纯水中诱导苯酚矿化的程度较低。氧化物表面的铁浸出非常有限,远低于废水排放标准。在天然水基质中,磁铁矿/过硫酸盐体系的合理性能和溶解态铁的低水平,对于去除废水中的有机污染物具有重要意义。