Assessment of perfluorocarboxylic acids in fluorinated high-density polyethylene containers and estimation of potential non-cancer risks associated with anticipated use scenarios.

High density polyethylene (HDPE) containers are fluorinated to impart barrier properties that prevent permeation of liquid products filled in the container. The process of fluorination may result in the unintentional formation of certain per- and polyfluoroalkyl substances (PFAS), specifically perfluoroalkyl carboxylic acids (PFCAs), as impurities. This study measured the amounts of PFCAs that may be present in the fluorinated HDPE containers, which could migrate into products stored in these containers. Migration studies were also conducted using water and mineral spirits to estimate the amount of PFCAs that might be found in the products stored in these containers. The migration results were used to conservatively model potential PFCA exposures from use of six product types: indoor-sprayed products, floor products, hand-applied products, manually-sprayed pesticides, hose-end sprayed products, and agricultural (industrial) pesticides. The potential that such uses could result in a non-cancer hazard was assessed by comparing the modeled exposures to both applicable human non-cancer toxicity values and environmental screening levels. Environmental releases were also compared to aquatic and terrestrial predicted no-effect concentrations (PNECs). The results of these analyses indicated no unreasonable non-cancer risk to humans, aquatic species, and terrestrial species from PFCAs in products stored in fluorinated HDPE containers.

Exposure monitoring toward environmental justice.

Executive Order 14008, signed on 27 January 2021, established environmental justice (EJ) as a core priority of the Biden Administration. There is a need for state and federal regulators, as well as industry, to enhance risk assessment methods and exposure monitoring approaches to be more inclusive of EJ community involvement and more representative of EJ community exposures. Cumulative risk assessment models are critical for understanding the unique interaction between chemical exposures and nonchemical stressors that EJ communities encounter daily. Enhanced environmental monitoring with personal and portable sensors, especially when deployed using community partnerships, can capture chemical exposures with sufficient resolution to characterize exposures down to the neighborhood level. Use of internet-linked sensors will also require thoughtful advances in management of big data to inform meaningful and time-sensitive decisions. Integr Environ Assess Manag 2022;18:858-862. © 2021 SETAC.

Advanced oxidation degradation kinetics as a function of ultraviolet LED duty cycle.

Ultraviolet (UV) light emitting diodes (LEDs) may be a viable option as a UV light source for advanced oxidation processes (AOPs) utilizing photocatalysts or oxidizing agents such as hydrogen peroxide. The effect of UV-LED duty cycle, expressed as the percentage of time the LED is powered, was investigated in an AOP with hydrogen peroxide, using methylene blue (MB) to assess contaminant degradation. The UV-LED AOP degraded the MB at all duty cycles. However, adsorption of MB onto the LED emitting surface caused a linear decline in reactor performance over time. With regard to the effect of duty cycle, the observed rate constant of MB degradation, after being adjusted to account for the duty cycle, was greater for 5 and 10% duty cycles than higher duty cycles, providing a value approximately 160% higher at 5% duty cycle than continuous operation. This increase in adjusted rate constant at low duty cycles, as well as contaminant fouling of the LED surface, may impact design and operational considerations for pulsed UV-LED AOP systems.

Comparison of continuous versus pulsed ultraviolet light emitting diode use for the inactivation of Bacillus globigii spores.

Light emitting diodes (LEDs) in the ultraviolet (UV) range offer a promising alternative for the disinfection of water. LEDs have many advantages over conventional UV lamps but there are concerns related to the operating life of the LED lamps. In this project Bacillus globigii was inactivated using UV LED technology. The experimental strategy included using pulsed ultraviolet (PUV) output rather than continuous UV (CUV) current in order to reduce the power requirements and extend the life of the lamps. The kinetic profiles for CUV experiments reached 6-log inactivation faster than PUV at 9.1% duty cycle (approx. 840 vs. 5,000 s) but the PUV required lower fluence (365 vs. 665 J/m²). In addition, the inactivation rate constants associated with PUV were generally higher than those of CUV (4.6-5.1 vs. 3.6-4.4 m²/J), which supports the notion that high energy bursts are more effective at causing cellular damage. Multi-target kinetics applied to most of the kinetic observations and tailing effects were generally observed. PUV LED appears to have potential to extend the lifetime of the LEDs for inactivation of spore-forming pathogens.

Detecting recalcitrant organic chemicals in water with microbial fuel cells and artificial neural networks.

This study integrates artificial neural network (ANN) processing with microbial fuel cell (MFC)-based biosensing in the detection of three organic pollutants: aldicarb, dimethyl-methylphosphonate (DMMP), and bisphenol-A (BPA). Overall, the use of the ANN proved to be more reliable than direct correlations for the determination of both chemical concentration and type. The ANN output matched the appropriate chemical concentration and type for three different concentrations and throughout a wide range of stepwise tests. Additionally, chemicals dissolved in the acetate-based feed medium (FM) were accurately identified by the ANN even though the acetate masked the pollutants' effects on electrical current. The ANN also accurately revealed the identity of chemical mixtures. This study is the first to incorporate ANN modeling with MFC-based biosensing for the detection and quantification of organic pollutants that are not readily biodegradable. Furthermore, this work provides insight into the flexibility of MFC-based biosensing as it pertains to limits of detection and its applicability to scenarios where mixtures of pollutants and unique solvents are involved. This research effort is expected to serve as a guide for future MFC-based biosensing efforts.

Evaluation of activated sludge for biodegradation of propylene glycol as an aircraft deicing fluid.

Aircraft deicing fluid used at airport facilities is often collected for treatment or disposal in order to prevent serious ecological threats to nearby surface waters. This study investigated lab scale degradation of propylene glycol, the active ingredient in a common aircraft deicing fluid, by way of a laboratory-scale sequencing batch reactor containing municipal waste water treatment facility activated sludge performing simultaneous organic carbon oxidation and nitrification. The ability of activated sludge to remove propylene glycol was evaluated by studying the biodegradation and sorption characteristics of propylene glycol in an activated sludge medium. The results indicate sorption may play a role in the fate of propylene glycol in AS, and the heterotrophic bacteria readily degrade this compound. Therefore, a field deployable bioreactor may be appropriate for use in flight line applications.

Fate of malathion and a phosphonic acid in activated sludge with varying solids retention times.

This study examined the ability of activated sludge (AS) to sorb and biodegrade ethylmethylphosphonic acid (EMPA) and malathion, a degradation product and surrogate, respectively, for an organophosphate chemical warfare agent. Sorption equilibrium isotherm experiments indicate that sorption of EMPA and malathion to AS is negligible. EMPA at a concentration of 1 mg L(-1) degraded by approximately 30% with apparent first-order kinetics, possibly via co-metabolism from nitrification. Heterotrophic bacteria and abiotic mechanisms, however, are largely responsible for malathion degradation also with apparent first-order kinetics. EMPA did not inhibit chemical oxygen demand (COD) oxidation or nitrification activity, although malathion did appear to induce a stress response resulting in inhibition of COD oxidation. The study also included a 30-day experiment in which malathion, at a concentration of 5 mg L(-1), was repeatedly fed to AS in bench-scale sequencing batch reactors (SBRs) operating at different solids retention times (SRTs). Peak malathion concentrations occurred at day 4.5, with the longer SRTs yielding greater peak malathion concentrations. The AS reduced the malathion concentrations to nearly zero by day 10 for all SRTs, even when the malathion concentration in the influent increased to 20.8 mg L(-1). The data suggest a biodegradation pathway for malathion involving an oxygenase. Phylogenetic analyses revealed that all samples had an abundance of Zoogloea, though there was greater bacterial diversity in the SBR with the SRT of 50 days. The SBR with an SRT of 9.5 days had an apparent reduction in the diversity of the bacterial community.

Fate of selected estrogens in two laboratory scale sequencing batch reactors fed with different organic carbon sources under varying solids retention times.

This study compared the performances of two laboratory-scale sequencing batch reactors to remove 17ß-estradiol and 17α-ethinyl estradiol. Both SBRs were operated to achieve organic carbon oxidation and nitrification. However, the overall bacterial population in both SBRs was targeted to be different by feeding the SBRs with peptone and glucose. Furthermore, the reactors were also run at different solid retention times (SRTs) to evaluate the effect of SRT on estrogen removal. The more diverse heterotrophic and ammonia oxidizing bacterial community in the peptone fed SBR1 had superior estrogen removal than the glucose fed SBR 2 which enriched less diverse community, particularly for 17α-ethinyl estradiol. Under a solids retention time (SRT) of 40days, the total 17ß-estradiol mass was 30% of the amount under the SRT of 20days, and the total 17α-ethinyl estradiol mass was likewise 40% of the amount under the shorter SRT.

Seasonal variations of nitrifying community in trickling filter-solids contact (TF/SC) activated sludge systems.

Two full-scale trickling filter/solids contact (TF/SC) basin plants, each successfully performing nitrification, were sampled throughout various seasons over a period of one year. Concentrations of ammonia, nitrate and nitrite were measured at various sampling locations along the treatment train. DNA was also extracted from mixed liquor in the solids contact basins. These DNA samples were subjected to terminal restriction fragment length polymorphism (TRFLP) in order to profile the ammonia oxidizing bacteria and nitrite oxidizing bacteria communities. In both plants, there was a prevalence of Nitrosomonas europaea among the ammonia oxidizing bacteria (AOBs). However, during the summer months, there was increased diversity of Nitrosomonas species. Likewise, Nitrospira spp. was the dominant nitrite oxidizing bacteria (NOBs) in both plants regardless of season. Yet there was an increased presence of Nitrobacter among the NOBs in the summer months. These results add an important understanding of the ecology and dynamics in nitrifying population in full-scale TF/SC wastewater treatment plants.

Effect of organic carbon on ammonia oxidizing bacteria in a mixed culture.

This study examined the effect of organic carbon (peptone vs. glucose) on two sequencing batch reactors performing simultaneous carbon oxidation and nitrification. Although each reactor had similar COD oxidation kinetics (0.029 and 0.036 mg COD mg VSS(-1) h(-1)), the Monod nitrification kinetics for the peptone-fed reactor (mu(m)=2.72 h(-1), K(s)=17.8 mg N L(-1)) were faster than for the glucose-fed reactor (mu(m)=0.868 h(-1), K(s)=26.5 mg L(-1)). The overall bacterial communities were profiled by 16S rRNA cloning and sequencing and revealed homology with a greater variety of bacteria from the peptone-fed reactor than the glucose-fed reactor. In addition, amoA cloning and sequencing, terminal restriction fragment length polymorphism, and fluorescent in situ hybridization experiments indicated greater AOB diversity and abundance in the peptone-fed reactor. This research provides evidence that the organic carbon source affects the make-up of the heterotroph community as well as AOB in mixed cultures.

Fate and removal of estrogens in municipal wastewater.

Natural and synthetic estrogens are some of the most potent endocrine disrupting compounds found in municipal wastewater. Much research has been conducted on the source and fate of estrogens in wastewater treatment plants. Sorption and biodegradation are the primary removal mechanisms for estrogens in activated sludge systems, which are widely used biological treatment techniques for municipal wastewater treatment. However, when removal of estrogens in a wastewater treatment plant is incomplete, these compounds enter the environment through wastewater discharges or waste activated sludge at concentrations that can cause endocrine-reproductive system alterations in birds, reptiles and mammals. Therefore, studies have also focused on potential advanced treatment technologies with the aim of removing the compounds before discharging wastewater effluent or disposing waste sludge. This review discusses the physiological effects of these estrogens and the degree of problems estrogens pose as they enter the wastewater stream. Thereafter, this review also analyzes their fate in wastewater treatment systems and how they may reach drinking water sources. Furthermore, this review includes a discussion on various treatment technologies being investigated and future research trends for this pressing environmental issue.