Evaluating UV₂₅₄ absorbance reductions in landfill leachate for municipal sewage co-treatment through timed UV/electrooxidation

Landfill leachate contains dissolved organic matter (DOM) exhibiting high ultraviolet absorbance at 254 nm (UVA₂₅₄). The UVA₂₅₄ limits leachate co-treatment with municipal sewage by hindering the downstream UV disinfection efficiency at wastewater treatment plants. Here, we alleviated the UVA₂₅₄ by timing the radiation in a UV/electrooxidation (UV/EO) process to accelerate reactive species formation. At 200 A·m⁻², the UV radiation was delayed by 10 min to accumulate 21 mg·L⁻¹ as Cl₂, which enhanced the initial radical formation rate by 5.25 times compared with a simultaneous UV/EO. The timed operation increased the steady-state concentrations of ClO^• by 700 times to 4.11 × 10⁻¹⁴ M and reduced the leachate UVA₂₅₄ by 78.2% after 60 min. We identified that aromatic formulas with low oxygen content were susceptible to UV/EO from Fourier-transform ion cyclotron resonance mass spectrometry analysis. The toxicity of the treated leachate and generated byproducts was assessed through specific oxygen uptake rates (SOUR) and developmental assays with Platynereis dumerilii. After quenching the residual chlorine, leachate co-treatment at 3.5% v/v presented minimal toxicological risk. Our findings provide operational insights for applying UV/EO in high UVA₂₅₄ matrices such as landfill leachate.