Per- and polyfluoroalkyl substances fate and transport at a wastewater treatment plant with a collocated sewage sludge incinerator.

This study aims to understand the fate and transport of per- and polyfluoroalkyl substances (PFAS) and inorganic fluoride (IF) at an undisclosed municipal wastewater treatment plant (WWTP) operating a sewage sludge incinerator (SSI). A robust statistical analysis characterized concentrations and mass flows at all WWTP and SSI primary influents/effluents, including thermal-treatment derived airborne emissions. WWTP-level net mass flows (NMFs) of total PFAS were not statistically different from zero. SSI-level NMFs indicate that PFAS, and specifically perfluoroalkyl acids (PFAAs), are being broken down. The NMF of perfluoroalkyl sulfonic acids (PFSAs; -274 ± 34 mg/day) was statistically significant. The observed breakdown primarily occurred in the sewage sludge. However, the total PFAS destruction and removal efficiency of 51 % indicates the SSI may inadequately remove PFAS. The statistically significant IF source (NMF = 16 ± 4.2 kg/day) compared to the sink of PFAS as fluoride (NMF = -0.00036 kg/day) suggests that other fluorine-containing substances are breaking down in the SSI. WWTP PFAS mass discharges were primarily to the aquatic environment (>99 %), with <0.5 % emitted to the atmosphere/landfill. Emission rates for formerly phased-out PFOS and PFOA were compared to previously reported levels. Given the environmental persistence of these compounds, the observed decreases in PFOS and PFOA discharge rates from prior reports implies regional/local differences in emissions or possibly their accumulation elsewhere. PFAS were observed in stack gas emissions, but modestly contributed to NMFs and showed negligible contribution to ambient air concentrations observed downwind.

Concentration profiles of per- and polyfluoroalkyl substances in major sources to the environment.

A review of published literature was conducted to present the concentrations and composition profiles of per- and polyfluoroalkyl substances (PFAS) from significant sources to the environment. The major sources of PFAS to the environment are categorized under direct and indirect sources. The characteristic compounds and concentrations are summarized as found from direct sources such as manufacturing facilities, aqueous film-forming foam (AFFF) applications, metal coating operations, and textile and paper coating operations; and from indirect sources such as landfills and wastewater treatment plants (WWTPs). The major findings are: 1) among the aqueous matrices for which data were reviewed, groundwater impacted by AFFF contamination showed the highest median concentrations for both perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic acid (PFOS), while the second-highest median concentrations were associated with landfill leachates for PFOA and metal-plating sources for PFOS; 2) many of the unknown polyfluorinated precursors present in AFFF-impacted sites could potentially convert to persistent PFAS by abiotic or biotic transformation, and therefore could act as the long-term source of contamination to the environment; 3) part per billion (ppb) concentrations of PFAS were detected in water bodies surrounding fluorochemical manufacturing plants; 4) in consumer products such as textile, paper, and personal care products, PFOA concentrations were an order of magnitude higher compared to other PFAS; 5) biotransformation products such as fluorotelomer carboxylic acids (FTCAs) and perfluoroalkyl acids (PFAAs) are detected in landfill leachates and WWTP effluents; and 6) many studies have shown increased PFAA concentrations in WWTP effluents compared to influents. This work provides a comprehensive review of the literature on the PFAS concentration and composition trends of select non-polymeric PFAS in different sources.

Impact of South Asian brick kiln emission mitigation strategies on select pollutants and near-term Arctic temperature responses.

The brick kiln industrial sector in South Asia accounts for large amounts of short-lived climate forcer (SLCF) emissions, namely black carbon (BC), organic carbon (OC), and sulfur dioxide (SO2; the precursor to atmospheric sulfate [SO4]). These SLCFs are air pollutants and have important impacts on both human health and the Arctic, a region currently experiencing more than double the rate of warming relative to the global average. Using previously derived Arctic equilibrium temperature response factors, we estimate the contribution to Arctic temperature impacts from previously reported emissions of BC, OC, and SO2 from four prevalent South Asian brick kiln types (Bull's Trench [BTK], Down Draught [DDK], Vertical Shaft [VSBK], and Zig-zag). Net annual BC (115 gigagrams [Gg]), OC (17 Gg), and SO2 (350 Gg) baseline emissions from all four South Asian kiln types resulted in 3.36 milliKelvin (mK) of Arctic surface warming. Given these baseline emissions and Arctic temperature responses, we estimate the current and maximum potential emission and temperature mitigation considering two kiln type conversions. Assuming no change in brick production, baseline emissions have been reduced by 17% when considering current BTK to Zig-zag conversions and have the potential to decrease by 82% given a 100% future conversion rate. This results in a 25% and 119% reduction in Arctic warming, respectively. Replacing DDKs with VSBKs increases baseline SLCF emissions by 28% based on current conversions and has the potential to increase by 131%. This conversion still reduces baseline warming by 31% and 149%, respectively. These results show that brick kiln conversions can have different impacts on local air quality and Arctic climate. When considering brick kiln emissions mitigation options, regional and/or local policy action should consider several factors, including local air quality, worker health and safety, cost, quality of bricks, as well as global climate impacts.

Estimating Arctic Temperature Impacts from Select European Residential Heating Appliances and Mitigation Strategies.

The use of residential heating devices is a key source of black carbon and other short-lived climate forcer emissions in Arctic and other high latitude regions, with important impacts to the Arctic climate and human health. The types of combustion technologies and fuels used varies by region, which impacts the emission profiles of these pollutants and thus the magnitude of Arctic climate responses. Using emission inventory data from 14 European countries, we derive wood-fueled residential heating emissions of black carbon, organic carbon, and sulfate from six appliance types in 2016. Using previously derived equilibrium Arctic temperature responses, we estimate Arctic temperature influences from each appliance type. Using the 2016 appliance emission data as a baseline, we compute the emission mass and Arctic temperature mitigation potential from hypothetical stove conversion scenarios. A total of 43.2 gigagrams (Gg) of black carbon, 175.7 Gg of organic carbon, and 10.3 Gg of sulfate were emitted in 2016 from the six appliance types in the 14 countries. The combined emissions increased Arctic surface temperatures by +2.8 millikelvin. If each country converted its appliance fleet to the technologically advanced pellet stoves and boilers, the combined black carbon, organic carbon, and sulfate emissions from heating appliances could be reduced by 94% and the Arctic temperature response reduced by 85%. The specific source and originating region of emissions are important factors in resolving the magnitude of their impacts. Improved country-level accounting of specific appliances and their emission characteristics can lead to a better understanding of potential mitigation options.