Grupo de investigación de análisis, tratamiento, electroquímica, recuperación y reúso de agua, WATER(2). Departamento de química inorgánica, Facultad de química y Farmacia, Pontificia Universidad Católica de Chile (PUC), Chile; Centro de Investigación de Procesos Redox, Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile (Uch), Santiago, Chile; Departamento de Química de los Materiales, Facultad de Química y Biología. Universidad de Santiago de Chile (USACH), Santiago, Chile.
Instituto de Química, Universidade Estadual Paulista (UNESP), Rua Professor Francisco Degni, 55, Araraquara, 14800-060, São Paulo, Brazil.
Chemosphere. 2024 Sep;364:143049. doi: 10.1016/j.chemosphere.2024.143049. Epub 2024 Aug 13.
The presence of persulfate (SO) in decontamination processes favors the oxidation of organic pollutants due to its strong oxidation power. In this research we study the photoelectrochemical generation of persulfate using five mixed metal oxides electrodes (MMO) with different compositions and its effect on the degradation of sulfamethoxazole antibiotic (SMX) by photoelectrocatalysis (PEC) and electro-oxidation (EO). By PEC, all anodes generated a higher concentration of SO than those not exposed to light. The high SOconcentration obtained by PEC was 0.150 mM using MMO in a solution with NaSO 100 mM applying a current density of 2 mA/cm. On the other hand, the maximum concentration obtained was 0.250 mM at 30 min of electrolysis for MMO using NaSO 50 mM and applying current density of 5 mA/cm. SOproduction by EO was between 0.005 and 0.089 mM. It is observed that MMO based in TaO showed the best SO production. The effect of SO electro-generation (using the anode with the highest and the anode with the lowest SO production) on the degradation of sulfamethoxazole by PEC and EO was studied using the experimental conditions with the best production of this oxidant. MMO and MMO were used as anodes, and it was observed that by PEC, 100% of SMX was degraded after 30 min of electrolysis using MMO and 60 min using MMO By EO, the degradation of SMX was partial, demonstrating that the electrophotocatalytic effect favors the generation of SO, enhancing the degradation of SMX at short electrolysis times.
过硫酸盐(SO)在去污过程中的存在由于其强大的氧化能力而有利于有机污染物的氧化。在这项研究中,我们研究了使用具有不同组成的五种混合金属氧化物电极(MMO)光电化学产生过硫酸盐及其对磺胺甲恶唑抗生素(SMX)的光电化学(PEC)和电氧化(EO)降解的影响。通过 PEC,所有阳极产生的 SO 浓度均高于未暴露于光的阳极。通过在 100 mM NaSO 溶液中使用 MMO 并施加 2 mA/cm 的电流密度,PEC 获得的高 SO 浓度为 0.150 mM。另一方面,在使用 50 mM NaSO 和施加 5 mA/cm 的电流密度进行 30 分钟电解时,MMO 获得的最大浓度为 0.250 mM。EO 产生的 SO 浓度在 0.005 和 0.089 mM 之间。观察到基于 TaO 的 MMO 显示出最佳的 SO 生产。使用具有最高和最低 SO 生产的阳极进行 SO 电生成(使用阳极)对 PEC 和 EO 降解磺胺甲恶唑的影响进行了研究,使用最佳生产氧化剂的实验条件。使用 MMO 和 MMO 作为阳极,观察到通过 PEC,在使用 MMO 进行 30 分钟电解后,SMX 的 100%被降解,而使用 MMO 则需要 60 分钟。通过 EO,SMX 的降解是部分的,这表明光电催化效应有利于 SO 的生成,在短时间电解下增强了 SMX 的降解。