State Key Laboratory of Urban Water Resources and Environment, School of Environment, Harbin Institute of Technology, Harbin, 150090, China.
State Key Laboratory of Urban Water Resources and Environment, School of Environment, Harbin Institute of Technology, Harbin, 150090, China.
Water Res. 2024 Jun 15;257:121684. doi: 10.1016/j.watres.2024.121684. Epub 2024 May 8.
Natural manganese oxides could induce the intermolecular coupling reactions among small-molecule organics in aqueous environments, which is one of the fundamental processes contributing to natural humification. These processes could be simulated to design novel advanced oxidation technology for water purification. In this study, periodate (PI) was selected as the supplementary electron-acceptor for colloidal manganese oxides (Mn(IV)) to remove phenolic contaminants from water. By introducing polyferric sulfate (PFS) into the Mn(IV)/PI system and exploiting the flocculation potential of Mn(IV), a post-coagulation process was triggered to eliminate soluble manganese after oxidation. Under acidic conditions, periodate exists in the HIO form as an octahedral oxyacid capable of coordinating with Mn(IV) to form bidentate complexes or oligomers (Mn(IV)-PI*) as reactive oxidants. The Mn(IV)-PI* complex could induce cross-coupling process between phenolic contaminants, resulting in the formation of oligomerized products ranging from dimers to hexamers. These oligomerized products participate in the coagulation process and become stored within the nascent floc due to their catenulate nature and strong hydrophobicity. Through coordination between Mn(IV) and HIO, residual periodate is firmly connected with manganese oxides in the floc after coagulation and could be simultaneously separated from the aqueous phase. This study achieves oxidizing oligomerization through a homogeneous process under mild conditions without additional energy input or heterogeneous catalyst preparation. Compared to traditional mineralization-driven oxidation techniques, the proposed novel cascade processes realize transformation, convergence, and separation of phenolic contaminants with high oxidant utilization efficiency for low-carbon purification.
天然锰氧化物可以在水相环境中诱导小分子有机物的分子间偶联反应,这是自然腐殖化的基本过程之一。这些过程可以被模拟,以设计用于水净化的新型高级氧化技术。在这项研究中,高碘酸盐(PI)被选为胶体锰氧化物(Mn(IV))的补充电子受体,以去除水中的酚类污染物。通过将聚硫酸铁(PFS)引入 Mn(IV)/PI 体系并利用 Mn(IV)的絮凝潜力,在氧化后引发后混凝过程以去除可溶性锰。在酸性条件下,高碘酸盐以 HIO 的形式存在,作为八面体含氧酸,能够与 Mn(IV)配位形成双齿配合物或低聚物(Mn(IV)-PI*)作为反应性氧化剂。Mn(IV)-PI* 配合物可以诱导酚类污染物之间的交叉偶联过程,导致形成从二聚体到六聚体的齐聚产物。这些齐聚产物由于其链状性质和强疏水性,参与混凝过程并作为存储在新生絮体中。通过 Mn(IV)和 HIO 的配位,剩余的高碘酸盐在混凝后与锰氧化物牢固地连接在絮体中,并可以与水相同时分离。本研究在温和条件下通过均相过程实现了氧化齐聚,无需额外的能量输入或异相催化剂制备。与传统的矿化驱动氧化技术相比,所提出的新型级联过程实现了酚类污染物的转化、收敛和分离,具有高氧化剂利用率和低碳净化。