School of Resource and Environmental Sciences, Hubei International Scientific and Technological Cooperation Base of Sustainable Resource and Energy, Wuhan University, Wuhan 430079, China.
State Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences, Beijing 100012, China.
Environ Sci Technol. 2020 Aug 18;54(16):10279-10288. doi: 10.1021/acs.est.0c00826. Epub 2020 Aug 10.
Dissolved silicate is an important background constituent of natural waters, but there is little clarity regarding the effect of silicate on the oxidizing capability of permanganate (Mn(VII)) and on its efficiency for remediation applications. In the present study, we found that dissolved silicate, metasilicate or disilicate (DS), could significantly promote the oxidation of 2,4-dichlorophenol (2,4-DCP) by Mn(VII), and the extent of the promoting effect was even more evident than that of pyrophosphate (PP). The experiments showed that, unlike PP, DS was not capable of coordinating with Mn(III) ions, and the promoting effect of DS was not due to the oxidizing capability of complexed Mn(III). Instead, DS ions, as a weak base, could combine with the hydroxyl groups of MnO via hydrogen bonding to limit the growth of colloidal MnO particles. The DS-stabilized colloidal MnO particles, with hydrodynamic diameters less than 100 nm, could act as catalysts to enhance the oxidation of 2,4-DCP by Mn(VII). The best promoting effect of DS on the performance of Mn(VII) oxidant was achieved at the initial solution pH of 7, and the coexisting bicarbonate ions further improved the oxidation of 2,4-DCP in the Mn(VII)/DS system. Sand column experiments showed that the combined use of Mn(VII) and DS additive could mitigate the problem of permeability reduction of sand associated with the retention of MnO particles. This study not only deepens our understanding on the role of dissolved silicate in a Mn(VII) oxidation process but also provides an effective and green method to enhance the oxidizing capacity of Mn(VII)-based treatment systems.
溶解态的硅酸盐是天然水体的一个重要背景组成部分,但关于硅酸盐对高锰酸盐(Mn(VII))氧化性的影响及其在修复应用中的效率,仍存在一些模糊认识。在本研究中,我们发现溶解态的硅酸钠、偏硅酸钠或二硅酸钠(DS)可以显著促进 Mn(VII)对 2,4-二氯苯酚(2,4-DCP)的氧化,其促进作用的程度甚至比焦磷酸根(PP)更为显著。实验表明,与 PP 不同,DS 不能与 Mn(III)离子配位,DS 的促进作用不是由于复合 Mn(III)的氧化性。相反,DS 离子作为弱碱,可以通过氢键与 MnO 的羟基结合,从而限制胶体 MnO 颗粒的生长。DS 稳定的胶体 MnO 颗粒,其水动力学直径小于 100nm,可以作为催化剂,增强 Mn(VII)对 2,4-DCP 的氧化。DS 对 Mn(VII)氧化剂性能的最佳促进效果是在初始溶液 pH 值为 7 时达到的,共存的碳酸氢根离子进一步提高了 Mn(VII)/DS 体系中 2,4-DCP 的氧化效率。砂柱实验表明,Mn(VII)和 DS 添加剂的联合使用可以减轻 MnO 颗粒截留导致的砂渗透性降低的问题。本研究不仅加深了我们对溶解态硅酸盐在 Mn(VII)氧化过程中作用的认识,还为增强基于 Mn(VII)的处理系统的氧化能力提供了一种有效且绿色的方法。