Department of Environmental & Resource Engineering, Technical University of Denmark, DK-2800 Lyngby, Denmark.
Department of Physics, Technical University of Denmark, Lyngby, DK 2800, Denmark.
Water Res. 2024 May 1;254:121388. doi: 10.1016/j.watres.2024.121388. Epub 2024 Feb 27.
The periodate (PI)-based advanced oxidation process is valued for environmental remediation, but current activation methods involve high costs, secondary contamination risks, and limited applicability due to external energy inputs (e.g., UV), catalyst incorporation (e.g., Fe), or environmental modifications (e.g., freezing). In this work, novel bioelectric activation of PI using the electrons generated by electroactive bacteria was developed and investigated for rapid removal of carbamazepine (CBZ), achieving 100 %, 100 %, and 76 % removal efficiency for 4.22 µM of CBZ in 20 min at pH 2, 120 min at pH 6.4, and HRT of 30 min at pH 8.5, respectively, with a 1 mM PI dose and without an input voltage. It was deduced that electrons derived from bacteria could directly activate PI using Ti mesh electrodes and generate •IO via single electron transfer under strongly acidic conditions (e.g., pH 2). Nevertheless, under weak alkaline conditions (e.g., pH 8.5), biogenic electrons indirectly activated PI by generating OHvia 4ereduction at the Ti mesh cathode, resulting in the formation of •O and O. In addition to the metal cathode, a carbon-based cathode finely modulates the 2ereduction, yielding HO and activating PI to mainly form •OH. Moreover, primarily non-toxic IO was produced during treatment, while no detectable reactive iodine species (HOI, I, and I) were observed. Furthermore, the bioelectric activation of PI demonstrated its capability to remove various micropollutants present in secondary-treated municipal wastewater, showcasing its broad-spectrum degradation ability. This study introduces a novel, cost-effective, and environmentally friendly PI activation technique with promising applicability for micropollutant elimination in water treatment.
过碘酸盐(PI)基高级氧化工艺因其在环境修复方面的价值而受到重视,但目前的激活方法由于外部能源输入(例如 UV)、催化剂掺入(例如 Fe)或环境修改(例如冻结)而涉及高成本、二次污染风险和有限的适用性。在这项工作中,使用电活性细菌产生的电子开发了新型的 PI 生物电化学激活,并研究了其对卡马西平(CBZ)的快速去除,在 pH 2 下用 4.22 µM 的 CBZ 在 20 分钟内达到 100%、100%和 76%的去除效率,在 pH 6.4 下 120 分钟,在 pH 8.5 下 HRT 为 30 分钟,PI 剂量为 1 mM,无需输入电压。推断出细菌衍生的电子可以直接使用钛网电极激活 PI,并在强酸条件下(例如 pH 2)通过单电子转移生成•IO。然而,在弱碱性条件下(例如 pH 8.5),生物电子通过在钛网阴极还原 4 生成 OH,间接激活 PI,导致•O 和 O 的形成。除了金属阴极外,碳基阴极还可以精细调节 2 还原,产生 HO 和激活 PI 主要形成•OH。此外,在处理过程中主要产生无毒的 IO,而没有检测到任何可检测的反应性碘物种(HOI、I 和 I)。此外,PI 的生物电化学激活证明了其去除二级处理市政废水中存在的各种微污染物的能力,展示了其广谱降解能力。本研究介绍了一种新颖、经济高效且环保的 PI 激活技术,具有在水处理中去除微污染物的广阔应用前景。