Pyrite and PHBV combined as substrates for groundwater denitrification

Nitrate pollution in groundwater has steadily increased globally, posing a potential threat to human health. Introduction of exogenous electron donors can significantly enhance nitrogen removal from nitrate-contaminated groundwater. Yet, conventional individual autotrophic or heterotrophic denitrification approaches have the disadvantage of low efficiency or high cost. This study investigated the performance of a laboratory-scale solid-phase denitrification (SPD) permeable reactive barrier (PRB) using a polyhydroxybutyrate-co-valerate (PHBV)/pyrite mixture as an electron donor for groundwater denitrification. Two different mass ratios (1:1 and 1:2) were established for the experimental setup. The results showed that under influent levels between 20 and 37 mg·L-1, the PHBV/pyrite system at a ratio of 1:1 achieved a maximum nitrate removal efficiency of 97.03%, with a nitrate removal rate of 99.13 mg NO3--N NO3--N·L-1·d-1. Moreover, the PHBV/pyrite system at 1:2 reached 97.65% and 111.04 mg NO3--N·L-1·d-1 in terms of the optimum nitrate removal efficiency and rate. Dissolved organic carbon was undetectable in the effluent in both systems. The nitrate removal performance of the PHBV/pyrite system at 1:2 was superior to the one at 1:1, implying appropriate addition of pyrite in mixtrophic systems could enhance denitrification in groundwater. Additionally, the dominant genera identified were respectively Cloacibacterium and Acinetobacter in two systems, indicating that varying PHBV/pyrite ratios can modulate the succession of dominant nitrogenremoving microorganisms. Specifically, the system at 1:2 favoured aerobic microbial growth, thereby enhancing the efficiency of biological nitrogen removal. The findings have provided a valuable alternative for mixtrophic denitrification in in-situ remediation of nitrate-polluted groundwater.