4.5 Article

Distribution and fate of per- and polyfluoroalkyl substances (PFAS) in wastewater treatment facilities

Journal

ENVIRONMENTAL SCIENCE-PROCESSES & IMPACTS
Volume 23, Issue 6, Pages 903-913

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1em00032b

Keywords

-

Funding

  1. UNH Collaborative Research Excellence (CoRE) Initiative
  2. New Hampshire Sea Grant (NHSG) [R/HCE-9]
  3. UNH STAF fellowship

Ask authors/readers for more resources

PFAS, as a class of persistent, bioaccumulative, and toxic anthropogenic compounds, are of growing concern due to their widespread use. This study in six New Hampshire municipal WWTFs found that short-chain PFAS were dominant in influent and effluent, while long-chain compounds were prevalent in sludge. The TOP assay indicated a significantly lower proportion of oxidizable PFAS precursors in July influent and effluent compared to March.
Anthropogenic compounds known as per- and polyfluoroalkyl substances (PFAS) represent a major class of contaminants of emerging concern composed of nearly 5000 chemicals. Many PFAS are persistent, bioaccumulative and toxic, and their widespread use makes their environmental distribution a growing concern. Wastewater treatment facilities (WWTFs) are a conduit of PFAS to the environment, integrating common household products from municipal sewage, industrial wastewater sources, septic materials, and firefighting wastewaters in effluent and sludge. This study investigated the distribution and fate of twenty-four PFAS within six New Hampshire municipal WWTFs applying a range of biological and disinfection unit processes. PFAS quantification was conducted using two approaches: (1) liquid chromatography with tandem mass spectrometry (LC-MS/MS) of 24 known compounds and (2) a total oxidizable precursor assay (TOP assay) followed by LC-MS/MS to determine the total oxidizable PFAS concentration. Of the 24 PFAS analyzed, up to 7 and 12 constituents were detected in influent and effluent of WWTFs, respectively, with concentrations ranging from 30 to 128 ng L-1 in March. Effluent sigma PFAS concentration increased during July, with concentrations between 70 and 198 ng L-1 for the same detected constituents. Short-chain PFAS were dominant in both influent and effluent, while long-chain compounds dominated in WWTF sludge. The increase in terminal end-products after oxidation by the TOP assay indicates the presence of unquantified PFAS precursors in both influent and effluent. A significantly lower proportion of oxidizable PFAS precursors were detected in July influent and effluent relative to March, indicating a possible role of season or temperature on microbial transformation of these compounds prior to reaching WWTFs and during treatment. These results provide new insight into PFAS distribution and fate during two seasons in New England municipal WWTFs.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available