Departamento de Química, División de Ciencias Naturales y Exactas, Universidad de Guanajuato, Cerro de la Venada s/n, Pueblito de Rocha, 36040 Guanajuato, Mexico.
Departamento de Química, División de Ciencias Naturales y Exactas, Universidad de Guanajuato, Cerro de la Venada s/n, Pueblito de Rocha, 36040 Guanajuato, Mexico.
Chemosphere. 2024 Sep;363:142825. doi: 10.1016/j.chemosphere.2024.142825. Epub 2024 Jul 10.
Electrochemical oxidation (EO), electro-Fenton (EF), and photoelectro-Fenton (PEF) with a BDD anode have been comparatively assessed to remediate solutions of Red CL and/or Red WB azo dyes from real raw water. For the EO process in 50 mM NaSO at pH 3.0, the main oxidant was the heterogeneous OH generated at the anode, whereas in EF and PEF, the cathodic production of HO and the addition of 0.50 mM Fe catalyst additionally originated homogeneous OH that enhanced the oxidation of organics. In PEF, the solution was illuminated with a 6 W UVA light. An almost total discoloration was always found operating with a 1:1 mixture of 200 mg L of both dyes in 60 min, whose efficiency increased in the order of EO < EF < PEF. The HPLC analysis of the dye mixture treated by PEF disclosed that its degradation process agreed with its discoloration. A high 74% of COD was reduced due to the oxidative action of hydroxyl radicals and the photolysis of final Fe(III)-carboxylate species with UVA irradiation. The process was accompanied by an energy consumption of 0.76 kWh (g COD), a value similar to the energy consumed by the applied UVA light.
电化学氧化(EO)、电芬顿(EF)和掺硼金刚石(BDD)阳极光电芬顿(PEF)已被用于比较修复来自实际原水的红色 CL 和/或红色 WB 偶氮染料溶液。在 pH 值为 3.0 的 50 mM NaSO 中进行 EO 过程时,主要氧化剂是阳极生成的非均相 OH;而在 EF 和 PEF 中,阴极产生的 HO 和添加 0.50 mM Fe 催化剂另外产生了均相 OH,从而增强了有机物的氧化。在 PEF 中,溶液用 6 W UVA 光照射。用 60 分钟处理 200mg/L 两种染料的 1:1 混合物时,总是可以实现完全脱色,其效率按 EO < EF < PEF 的顺序增加。用 PEF 处理的染料混合物的 HPLC 分析表明,其降解过程与其脱色过程一致。由于羟基自由基的氧化作用和 UVA 照射下最终 Fe(III)- 羧酸盐物种的光解,COD 减少了 74%。该过程伴随着 0.76 kWh(g COD)的能耗,这一值与所应用的 UVA 光的能耗相似。