Release of poly- and perfluoroalkyl substances from finished biosolids in soil mesocosms

Finished biosolids were collected and characterized from seven municipal water resource recovery facilities. Poly-and perfluoroalkyl substances (PFAS) for the 54 quantified in the biosolids ranged from 323 +/- 14.1 to 1100 +/- 43.8 mu g/kg (dry weight basis). For all biosolids, greater than 75% of the PFAS fluorine mass was associated with precursors. Di-substituted polyfluorinated phosphate esters (diPAPs) were the most abundant PFAS identified in the biosolids. The total oxidizable precursor assay on biosolids extracts generally failed to quantify the amount of precursors present, in large part due to the fact that diPAPS were not fully transformed during the TOP assay. Outdoor biosolids column leaching experiments intended to simulate biosolids land application showed sustained PFAS leaching over the 6-month study duration. Perfluoroalkyl acid (PFAA) concentrations in leachate, when detected, typically ranged in the 10 s to 100 s of ng/L; no diPAPs were detected in the leachate. The PFAA leaching from the biosolids exceeded the PFAA mass initially present in the biosolids (typically by greater than an order of magnitude), but the cumulative PFAA mass leached did not exceed the molar equivalents that could be explained by transformation of quantified precursors. These results highlight the importance of PFAA precursors initially present in biosolids and their contribution to long term leaching of PFAAs from land-applied biosolids.

Automated summary

This study collected and characterized finished biosolids from seven municipal water resource recovery facilities. The results showed a significant presence of PFAS, with diPAPs being the most common. The total oxidizable precursor assay failed to accurately measure the amount of precursors in the biosolids. Leaching experiments simulating biosolids land application demonstrated sustained leaching of PFAS over a 6-month period.