磁铁矿
过氧二硫酸盐
化学
环境修复
吸附
无机化学
铜
催化作用
地下水修复
污染
材料科学
有机化学
冶金
生态学
生物
作者
Jiabin Chen,Xuefei Zhou,Yumin Zhu,Yalei Zhang,Ching‐Hua Huang
出处
期刊:Water Research
[Elsevier BV]
日期:2020-09-01
卷期号:186: 116371-116371
被引量:33
标识
DOI:10.1016/j.watres.2020.116371
摘要
Magnetite is known to exhibit high catalytic reactivity in Fenton-like reactions merely at low pH conditions. Here we report the association of Cu2+ ion can significantly enhance peroxydisulfate (PDS) activation with magnetite under environmental aquatic conditions (near neutral pH). Cu2+ is able to synergistically activate PDS with magnetite to generate radicals, e.g., SO4·−, at neutral or slightly alkaline pH, and such synergistic activation of PDS is promising to degrade various contaminants in groundwater. In-depth study reveals Cu2+ ion adsorbed on magnetite plays a crucial role in PDS activation. The adsorbed Cu2+ is labile to be reduced by the structural Fe(II) on magnetite to generate Cu+, which is relatively stable in the presence of magnetite at neutral or alkaline pH, but extremely unstable at acidic pH. The generated Cu+ on magnetite surface, rather than Cu2+, contributes to PDS activation in the reaction system, and the recycling of Cu+/Cu2+ sustains continuous activation of PDS. This study is among the first to report the synergistic activation of PDS by magnetite and Cu2+ ion at neutral pH, and unambiguously discern the role of Cu+ in PDS activation. The new mechanistic knowledge provides a more accurate understanding of PDS activation by natural minerals in environmental remediation.
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