State Key Laboratory of Pollution Control and Resources Reuse, College of Environmental Science and Engineering , Tongji University , Shanghai 200092 , P. R. China.
Shanghai Institute of Pollution Control and Ecological Security , Shanghai 200092 , P. R. China.
Environ Sci Technol. 2019 Sep 3;53(17):10227-10235. doi: 10.1021/acs.est.9b03456. Epub 2019 Aug 22.
The detection of soluble Mn(III) is typically accomplished using strong complexing agents to trap Mn(III), but the generation of soluble Mn(III) induced by strong complexing agents has seldom been considered. In this study, pyrophosphate (PP), a nonredox active ligand, was chosen as a typical Mn(III) chelating reagent to study the influence of ligands on soluble Mn(III) formation in reactions involving Mn oxides and Mn(VII). The presence of excess PP induced the generation of soluble Mn(III)-PP from α- and δ-MnO and led to the conproportionation reaction of α-, β-, δ-, or colloidal MnO with Mn(II) at pH 7.0. Compared to MnO minerals, colloidal MnO showed much higher reactivity toward Mn(II) in the presence of PP and the conproportionation rate of colloidal MnO with Mn(II) elevated with increasing PP dosage and decreasing pH. The generation of Mn(III) was not observed in MnO/SO or MnO/NHOH system without PP while the introduction of excess PP induced the generation of Mn(III)-PP. Thermodynamic calculation results were consistent with the experimental observations. These findings not only provide evidence for the unsuitability of using strong ligands in quantification of soluble Mn(III) in manganese-involved redox reactions, but also advance the understanding of soluble Mn(III) generation in aquatic environment.
可溶性 Mn(III)的检测通常采用强络合剂来捕获 Mn(III),但很少考虑强络合剂诱导的可溶性 Mn(III)的生成。在这项研究中,焦磷酸根 (PP) 作为一种典型的 Mn(III)螯合剂被选择来研究配体对 Mn 氧化物和 Mn(VII)参与的反应中可溶性 Mn(III)形成的影响。过量的 PP 的存在诱导了 α-和 δ-MnO 中可溶性 Mn(III)-PP 的生成,并导致 α-、β-、δ-或胶体 MnO 与 Mn(II)在 pH 7.0 下发生共配反应。与 MnO 矿物相比,胶体 MnO 在有 PP 存在的情况下对 Mn(II)表现出更高的反应活性,随着 PP 用量的增加和 pH 的降低,胶体 MnO 与 Mn(II)的共配反应速率升高。在没有 PP 的 MnO/SO 或 MnO/NHOH 体系中没有观察到 Mn(III)的生成,而过量的 PP 的引入诱导了 Mn(III)-PP 的生成。热力学计算结果与实验观察结果一致。这些发现不仅为在涉及锰的氧化还原反应中定量测定可溶性 Mn(III)时不使用强配体提供了证据,而且还提高了对水环境污染中可溶性 Mn(III)生成的认识。