Variable PFAS removal by adsorbent media with sufficient prediction of breakthrough despite reduced contact time at pilot scale.

One alternative adsorbent (AA) and five ion exchange (IX) resins were tested for the removal of per- and polyfluoroalkyl substances (PFAS) from groundwater in pilot-scale columns for up to 19 months using empty bed contact times (EBCTs) representative of full-scale treatment. For the six detected PFAS in the pilot feed water, the long-chain PFAS (perfluorooctanoic acid [PFOA], perfluorooctanesulfonic acid [PFOS], and perfluorohexanesulfonic acid [PFHxS]) were well removed with only PFOA, which is a perfluoroalkyl carboxylic acid (PFCA) eventually breaking through as the media became exhausted. Perfluorobutanesulfonic acid (PFBS), a short-chain perfluorosulfonic acid (PFSA), was also well removed, whereas short-chain PFCAs (perfluoropentanoic acid [PFPeA] and perfluorobutanoic acid [PFBA]) were not removed (i.e., immediate breakthrough). Overall, IX and AA demonstrated superior removal of PFSAs compared to PFCAs (i.e., later breakthrough of PFSAs translating to longer media life). Media life varied, ranging from 6 to 15 months before adsorbents reached a significant PFOA breakthrough. The performance of the two adsorbents piloted at shorter EBCT reasonably predicted the longer (representative) pilot EBCT results (within ±20-30%) for the same adsorbents following data scaling. This suggests that pilot-scale testing may be conducted at a faster pace and therefore more economically. PRACTITIONER POINTS: Long-chain PFAS (PFOA, PFOS, and PFHxS) were well removed by five ion exchange and one alternative adsorbent tested herein. One short-chain PFAS (PFBS) was well removed with no removal of two other short-chain PFAS (PFBA and PFPeA). Performance of the two adsorbents piloted at shorter EBCT reasonably predicted the longer (representative) pilot EBCT results for the same adsorbents following data scaling.

The Future of Municipal Wastewater Reuse Concentrate Management: Drivers, Challenges, and Opportunities.

Water reuse is rapidly becoming an integral feature of resilient water systems, where municipal wastewater undergoes advanced treatment, typically involving a sequence of ultrafiltration (UF), reverse osmosis (RO), and an advanced oxidation process (AOP). When RO is used, a concentrated waste stream is produced that is elevated in not only total dissolved solids but also metals, nutrients, and micropollutants that have passed through conventional wastewater treatment. Management of this RO concentrate─dubbed municipal wastewater reuse concentrate (MWRC)─will be critical to address, especially as water reuse practices become more widespread. Building on existing brine management practices, this review explores MWRC management options by identifying infrastructural needs and opportunities for multi-beneficial disposal. To safeguard environmental systems from the potential hazards of MWRC, disposal, monitoring, and regulatory techniques are discussed to promote the safety and affordability of implementing MWRC management. Furthermore, opportunities for resource recovery and valorization are differentiated, while economic techniques to revamp cost-benefit analysis for MWRC management are examined. The goal of this critical review is to create a common foundation for researchers, practitioners, and regulators by providing an interdisciplinary set of tools and frameworks to address the impending challenges and emerging opportunities of MWRC management.

Methyl nitrate as a byproduct in advanced water treatment systems: Liquid chromatographic determination method and cause of formation.

Neutral low-molecular-weight organics such as methyl nitrate that can readily pass through reverse osmosis (RO) membranes employed in potable water reuse facilities attract interest owing to public health considerations. In this study, a novel determination method based on high-performance liquid chromatography, online photochemical conversion to peroxynitrite, and luminol chemiluminescence detection was developed for methyl nitrate measurement in treated water. The maximum photochemical conversion efficiency of methyl nitrate to peroxynitrite was found to be 6.5% using a 222-nm excimer lamp. The calibration curve for the developed method was linear between 1.0 × 10-9 and 1.0 × 10-7 M, and the limit of detection was 0.3 nM (0.03 µg/L) given an injection volume of 200 µL. The methyl nitrate concentrations in RO permeate from reclaimed wastewater and product water after subsequent treatment by a UV/H2O2 advanced oxidation process (AOP) were 2.2 and 22.5 nM (0.17 and 1.7 µg/L), respectively. UV irradiation of RO permeate in the laboratory using a low-pressure Hg lamp confirmed the formation of methyl nitrate in the permeate in the absence of H2O2 and residual chloramines. This chemiluminescent detection method for methyl nitrate will promote a greater understanding of the origin and formation of this treatment byproduct in reclaimed wastewater.

SARS-CoV-2 genetic material is removed during municipal wastewater treatment and is undetectable after advanced treatment.

The aim of this study was to establish whether SARS-CoV-2 genetic material is detectable after municipal wastewater treatment and to verify its expected removal from purified water that is reclaimed for potable reuse. Viral loads of SARS-CoV-2 (N1 and N2 genes) were monitored in raw influent wastewater (sewage) entering a water reclamation facility and in subsequent advanced treatment. Despite the large viral RNA load in raw sewage during peak COVID-19 outbreaks, substantial amounts of SARS-CoV-2 genetic material were removed during the conventional wastewater treatment process. Further, SARS-CoV-2 genetic material was undetectable after advanced purification. This confirms that potable reuse is resilient against high viral loads which are expected results given the advanced degree of wastewater and water treatment. Findings from this study may enhance public perception of the safety of potable water reuse; however, it should also be noted that studies to date worldwide indicate no evidence of SARS-CoV-2 transmission via water, and the CDC does not consider fecal waste or wastewaters as a source of exposure.

Epoxy lining influence on recycled water quality during pipeline transit for potable reuse.

An epoxy treatment was applied to a pipeline used to convey advanced treated recycled water from a purification facility to a recharge site. The epoxy treatment was applied to prevent further deterioration (corrosion) of the interior cement mortar lining (CML). A soil column study was conducted to evaluate the effect of the epoxy liner on the clogging potential of water before and after conveyance. The clogging potential was represented by differences in the column's relative hydraulic conductivity and water quality, between the treatment plant and injection site, before and after epoxy lining. Hydraulic conductivity of columns at the injection well site declined rapidly before epoxy and improved considerably after epoxy application. Total suspended solids (TSS) and cellular adenosine triphosphate (cATP) median concentrations improved significantly. Before epoxy, TSS increased with pipeline transit from 0.005 to 0.053 (mg/L) compared with 0.009 mg/L after epoxy. Before epoxy, cATP increased from 0.14 to 1.6 pg/ml across pipeline transit compared with 0.37 pg/ml after epoxy. Aluminum and nitrate followed similar trends. Results indicate that epoxy liner reduced the clogging potential of high purity recycled water, likely due to a decrease in particle and biomass load (clogging constituents) accumulated during pipeline transit. PRACTITIONER POINTS: Clogging potential of advanced treated recycled water increases with pipeline transit. Epoxy lining the pipeline used for conveyance reduces the particulate and microbial loading of the highly purified water. Applying epoxy to pipelines used to convey advanced treated recycled water has the dual benefit of infrastructure protection and improving water quality. Reducing particle and microbial load in the advanced treated recycled water can reduce maintenance frequencies and elongate production periods for MAR applications.

Online colloidal particle monitoring for controlled coagulation pretreatment to lower microfiltration membrane fouling at a potable water reuse facility.

Fouling of microfiltration (MF)) membranes during water/wastewater treatment is predominantly caused by colloidal particles (size <1 µm) in the feed water. Until recently no online technology was available to directly measure the occurrence of colloidal particles in these waters. This study evaluated the viability of a novel online light scattering technology (Nanoparticle Tracking Analysis) to continuously monitor colloidal particles in the membrane feed water (a secondary-treated wastewater) for targeted removal by injecting coagulant at a dosage proportional to the measured concentration of colloidal particles. A diurnal variation was observed in the colloidal particle concentration in the feed water with the lowest concentration occurring at approximately 6 am and the highest concentration occurring after mid-day. The peak colloidal particle concentrations were 4 to 6 times higher than the lowest concentrations measured on the same day. Bench-scale studies were performed to develop a relationship between colloidal particle concentration and the optimum coagulant dosage required for their removal. Subsequently, a pilot-scale study was performed using two MF pilot units operated in parallel, one receiving targeted coagulant dosing and the other with no coagulant dosing, to demonstrate the effectiveness of targeted coagulant dosing in preventing membrane fouling. The pilot unit that received targeted coagulant dose experienced only 4 to 20% of the transmembrane pressure increase of the increase experienced by the pilot unit that received no coagulant. Evaluation of fouling resistance indicated that targeted coagulation improved flux by predominantly lowering the irreversible fouling. The filtrate water quality measured by colloidal particle concentration, chemical oxygen demand (COD), and turbidity were very similar for the two pilot units. This suggests that although the efficiency of particle and organic materials removal does not change with coagulant addition, the particles filtered by the membrane in the control unit contributed to membrane irreversible fouling, while in the coagulant-treated unit, the coagulated colloidal particles were removed away from the membrane into the backwash stream during the frequent backwash/air scour procedures.

NDMA and NDMA precursor attenuation in environmental buffers prior to groundwater recharge for potable reuse.

Natural attenuation of N-nitrosodimethylamine (NDMA) and NDMA precursors was evaluated in infiltration basins, a riverbed filtration system, and constructed wetlands operated as part of a managed aquifer recharge system. Initial NDMA concentrations up to 9.0 ng/L in infiltration basins (advanced purified, recycled water) before sunrise declined to non-detect (<1.5 ng/L) by 10:00 A.M due to natural photolysis (half-life of 33 to 86 min dependent on solar irradiance). NDMA fortified controls adjacent to the infiltration basin showed similar results, while concentrations in dark controls did not change over the basin's hydraulic retention time. NDMA precursor concentrations did not change significantly in the basin containing advanced-treated water from a potable reuse treatment plant, indicating that photolysis did not remove NDMA precursors nor did photolysis produce a significant amount of precursors. For the other environmental buffers evaluated, NDMA removal was variable through laboratory scale soil columns (22 cm height), in full-scale riverbed filtration system that pre-filters water prior to infiltration basin recharge, and in the constructed wetland. Variability in NDMA removal through the wetlands is attributed to high turbidity. In the case of the riverbed filtration system, variability is likely due to short exposure times to sunlight. For the soil columns, limited NDMA removal is attributed to inefficacy of soil aquifer treatment in removing NDMA over short travel times/distances. NDMA precursors were also ineffectively removed in these systems, with effluent concentrations occasionally exceeding influent concentrations. Overall, the removal of NDMA in environmental buffers utilized for planned or de facto indirect potable reuse is dependent on the system's capacity for photolysis, while NDMA precursors are more recalcitrant and unlikely to be removed in such systems without enhancement or sufficient hydraulic residence times.

Distributed Temperature Sensing to Measure Infiltration Rates Across a Groundwater Recharge Basin.

Managed aquifer recharge is used to augment groundwater resources and provide resiliency to water supplies threatened by prolonged droughts. It is important that recharge facilities operate at their maximum efficiency to increase the volume of water stored for future use. In this study, we evaluate the use of distributed temperature sensing (DTS) technology as a tool to measure high-resolution infiltration rates at a large-scale recharge facility. Fiber optic cable was laid out inside a spreading basin in a spiral pattern, at two different depths. The cables measured the propagation of diurnal surface water temperature oscillations into the basin depth. The rate of heat propagation is proportional to the velocity of the water, making it possible to estimate the infiltration rate from the temperature measurements. Our results showed that the infiltration rate calculated from DTS, averaged over the entire basin, was within 5% of the infiltration rate calculated using a conventional metering method. The high-resolution data obtained from DTS, both spatially and temporally, revealed heterogeneous infiltration rates throughout the basin; furthermore, tracking the evolution of infiltration rates over time revealed regions with consistently high infiltration rates, regions with consistently low infiltration rates, and regions that evolved from high to low rates, which suggested clogging within that region. Water utilities can take advantage of the high-resolution information obtained from DTS to better manage recharge basins and make decisions about cleaning schedule, frequency, and extent, leading to improved basin management strategies, reduced O&M costs, and increased groundwater recharge.

Pilot-scale evaluation of oxidant speciation, 1,4-dioxane degradation and disinfection byproduct formation during UV/hydrogen peroxide, UV/free chlorine and UV/chloramines advanced oxidation process treatment for potable reuse.

Advanced oxidation using UV/free chlorine and UV/chloramines are being considered as alternatives to UV/H2O2 for treatment of reverse osmosis (RO) permeate in treatment trains for the potable reuse of municipal wastewater. This pilot-scale comparison of the three advanced oxidation processes (AOPs) evaluated three factors important for selecting among these alternatives. First, the study characterized the speciation of oxidants serving as the source of radicals within the AOPs to facilitate process modeling. Kinetic modeling that included consideration of the chloramines occurring in RO permeate accurately predicted oxidant speciation. Modeling of the UV/free chlorine AOP indicated that free chlorine is scavenged by reactions with ammonia and monochloramine in RO permeate, such that oxidant speciation can shift in favor of dichloramine over the short (∼30 s) timescale of AOP treatment. Second, the order of efficacy for degrading the target contaminant, 1,4-dioxane, in terms of minimizing UV fluence was UV/free chlorine > UV/H2O2 ≫ UV/chloramines. However, estimates indicated that the UV/chloramines and UV/H2O2 AOPs could be similar on a cost-effectiveness basis due to savings in reagent costs by the UV/chloramines AOP, provided the RO permeate featured >3 mg/L as Cl2 chloramines. Third, the study evaluated whether the use of chlorine-based oxidants within the UV/free chlorine and UV/chloramines AOPs enhanced disinfection byproduct (DBP) formation. Even after AOP treatment and chloramination, total halogenated DBP formation remained low at <15 µg/L for all three AOPs. DBP formation was similar between the AOPs, except that the UV/free chlorine AOP promoted haloacetaldehyde formation, while the UV/H2O2 and UV/chloramines AOPs followed by chloramination increased chloropicrin formation. However, total DBP formation on a toxic potency-weighted basis was similar among the AOPs, since haloacetonitriles and haloacetamides were the dominant contributors and did not differ significantly among the AOPs.

Influence of reverse osmosis membrane age on rejection of NDMA precursors and formation of NDMA in finished water after full advanced treatment for potable reuse.

The influence of reverse osmosis (RO) membrane age on rejection of N-nitrosodimethylamine (NDMA) precursors was evaluated for a full-scale potable water reuse facility. The rejection of NDMA precursors decreased slightly with increased membrane age in most RO membrane products evaluated, but remained high overall (91% average). Chloride rejection was well-correlated with rejection of NDMA precursors. Precursor removal varied (75-98%) by membrane product, with certain membrane products maintaining better precursor rejection over time. NDMA rejection, however, did not decline significantly over time, while passage of other low molecular weight organics (LMWOs) increased with membrane age. Thus, rejection of NDMA was not highly correlated with rejection of these LMWOs, suggesting that NDMA is not a good surrogate for these compounds. Incomplete removal of NDMA precursors by RO and a UV/advanced oxidation process (UV/AOP) led to NDMA formation in the finished water and miles downstream in the transmission pipelines. An average NDMA formation rate of 0.7 ng/L/hr in the transmission lines was observed, despite typical removal of NDMA by UV/AOP to non-detect levels. The study indicates that RO membranes throughout their lifetime are not an absolute barrier to NDMA precursors, and that while older membranes continue to sufficiently remove NDMA precursors to a high degree, NDMA precursor rejection may decrease slightly as membranes age. Thus, the potential exists for NDMA to form from these precursors in purified, potable reuse water after treatment despite the effective removal of NDMA by UV/AOP.

Characterization of the Microbiome at the World's Largest Potable Water Reuse Facility.

Conventional water resources are not sufficient in many regions to meet the needs of growing populations. Due to cyclical weather cycles, drought, and climate change, water stress has increased worldwide including in Southern California, which serves as a model for regions that integrate reuse of wastewater for both potable and non-potable use. The Orange County Water District (OCWD) Advanced Water Purification Facility (AWPF) is a highly engineered system designed to treat and produce up to 100 million gallons per day (MGD) of purified water from a municipal wastewater source for potable reuse. Routine facility microbial water quality analysis is limited to standard indicators at this and similar facilities. Given recent advances in high throughput DNA sequencing techniques, complete microbial profiling of communities in water samples is now possible. By using 16S/18S rRNA gene sequencing, metagenomic and metatranscriptomic sequencing coupled to a highly accurate identification method along with 16S rRNA gene qPCR, we describe a detailed view of the total microbial community throughout the facility. The total bacterial load of the water at stages of the treatment train ranged from 3.02 × 106 copies in source, unchlorinated wastewater feed to 5.49 × 101 copies of 16S rRNA gene/mL after treatment (consisting of microfiltration, reverse osmosis, and ultraviolet/advanced oxidation). Microbial diversity and load decreased by several orders of magnitude after microfiltration and reverse osmosis treatment, falling to almost non-detectable levels that more closely resembled controls of molecular grade laboratory water than the biomass detected in the source water. The presence of antibiotic resistance genes and viruses was also greatly reduced. Overall, system design performance was achieved, and comprehensive microbial community analysis was found to enable a more complete characterization of the water/wastewater microbial signature.

An inline ion-exchange system in a chemiluminescence-based analyzer for direct analysis of N-nitrosamines in treated wastewater.

A newly developed, ion exchange-based inline pretreatment system was used to mitigate the effect of background constituents in natural water and treated wastewater to achieve rapid, reliable, and sensitive analysis of N-nitrosamines. The pretreatment system (anion exchange module, AEM) was incorporated into a high-performance liquid chromatograph (HPLC) coupled with a photochemical reactor (PR) and chemiluminescence (CL) detector (HPLC-PR-CL), which can analyze four hydrophilic N-nitrosamines at ng/L levels. This system requires no pre-concentration of the water sample nor the use of deuterated surrogates, unlike other conventional N-nitrosamine analytical techniques. The AEM converted anions in the eluent to hydroxide ions after HPLC separation and increased eluent pH, allowing for the subsequent photochemical reactions, which are otherwise achieved by pH conditioning with an additional dosing pump of basic chemical. The AEM also removed anionic interfering compounds (e.g. nitrate) from the samples, allowing for improved N-nitrosamine analysis in treated wastewater. The operating conditions of the AEM and PR were optimized to obtain sensitive and stable analytical performance. As a result, the lowest-concentration minimum reporting levels of N-nitrosodimethylamine, N-nitrosomorpholine, N-nitrosomethylethylamine, and N- nitrosopyrrolidine using the optimized system were 0.42, 0.54, 0.58, and 1.4 ng/L, respectively. The improved analytical method was validated by comparing the results with a conventional method based on gas chromatography coupled with a mass spectrometric ion trap detector. These results indicated that HPLC-PR-CL equipped with an inline AEM can be competitively applied as a rapid analytical technique for the determination of N-nitrosamines in various water matrices.

A review of polymeric membranes and processes for potable water reuse.

Conventional water resources in many regions are insufficient to meet the water needs of growing populations, thus reuse is gaining acceptance as a method of water supply augmentation. Recent advancements in membrane technology have allowed for the reclamation of municipal wastewater for the production of drinking water, i.e., potable reuse. Although public perception can be a challenge, potable reuse is often the least energy-intensive method of providing additional drinking water to water stressed regions. A variety of membranes have been developed that can remove water contaminants ranging from particles and pathogens to dissolved organic compounds and salts. Typically, potable reuse treatment plants use polymeric membranes for microfiltration or ultrafiltration in conjunction with reverse osmosis and, in some cases, nanofiltration. Membrane properties, including pore size, wettability, surface charge, roughness, thermal resistance, chemical stability, permeability, thickness and mechanical strength, vary between membranes and applications. Advancements in membrane technology including new membrane materials, coatings, and manufacturing methods, as well as emerging membrane processes such as membrane bioreactors, electrodialysis, and forward osmosis have been developed to improve selectivity, energy consumption, fouling resistance, and/or capital cost. The purpose of this review is to provide a comprehensive summary of the role of polymeric membranes in the treatment of wastewater to potable water quality and highlight recent advancements in separation processes. Beyond membranes themselves, this review covers the background and history of potable reuse, and commonly used potable reuse process chains, pretreatment steps, and advanced oxidation processes. Key trends in membrane technology include novel configurations, materials and fouling prevention techniques. Challenges still facing membrane-based potable reuse applications, including chemical and biological contaminant removal, membrane fouling, and public perception, are highlighted as areas in need of further research and development.

Economic and ecological costs and benefits of streamflow augmentation using recycled water in a California coastal stream.

Streamflow augmentation has the potential to become an important application of recycled water in water scarce areas. We assessed the economic and ecological merits of a recycled water project that opted for an inland release of tertiary-treated recycled water in a small stream and wetland compared to an ocean outfall discharge. Costs for the status-quo scenario of discharging secondary-treated effluent to the ocean were compared to those of the implemented scenario of inland streamflow augmentation using recycled water. The benefits of the inland-discharge scenario were greater than the increase in associated costs by US$1.8M, with recreational value and scenic amenity generating the greatest value. We also compared physical habitat quality, water quality, and benthic macroinvertebrate community upstream and downstream of the recycled water discharge to estimate the effect of streamflow augmentation on the ecosystem. The physical-habitat quality was higher downstream of the discharge, although streamflow came in unnatural diurnal pulses. Water quality remained relatively unchanged with respect to dissolved oxygen, pH, and ammonia-nitrogen, although temperatures were elevated. Benthic macroinvertebrates were present in higher abundances, although the diversity was relatively low. A federally listed species, the California red-legged frog (Rana draytonii), was present. Our results may support decision-making for wastewater treatment alternatives and recycled water applications in Mediterranean climates.

Recycled water for stream flow augmentation: benefits, challenges, and the presence of wastewater-derived organic compounds.

Stream flow augmentation with recycled water has the potential to improve stream habitat and increase potable water supply, but the practice is not yet well understood or documented. The objectives of this report are to present a short review illustrated by a case study, followed by recommendations for future stream flow augmentation projects. Despite the fact that wastewater discharge to streams is commonplace, a water agency pursuing stream flow augmentation with recycled water will face unique challenges. For example, recycled water typically contains trace amounts of organic wastewater-derived compounds (OWCs) for which the potential ecological risks must be balanced against the benefits of an augmentation project. Successful stream flow augmentation with recycled water requires that the lead agency clearly articulate a strong project rationale and identify key benefits. It must be assumed that the public will have some concerns about water quality. Public acceptance may be better if an augmentation project has co-benefits beyond maintaining stream ecosystems, such as improving water system supply and reliability (i.e. potable use offset). Regulatory or project-specific criteria (acceptable concentrations of priority OWCs) would enable assessment of ecosystem impacts and demonstration of practitioner compliance. Additional treatment (natural or engineered) of the recycled water may be considered. If it is not deemed necessary or feasible, existing recycled water quality may be adequate to achieve project goals depending on project rationale, site and water quality evaluation, and public acceptance.

Evaluation of hexavalent chromium in sediment pore water of the Hackensack River, New Jersey, USA.

Pore water was collected from in situ passive samplers in Hackensack River sediments adjacent to a chromite ore processing residue site in Kearny, New Jersey. Although the sediments at this site contained more than 3,000 mg/kg of total chromium (Cr) and shallow groundwater adjacent to the shore contained more than 1,000 microg/L of hexavalent Cr [Cr(VI)], concentrations of dissolved total Cr and Cr(VI) in pore water (PW) samples were less than ambient water quality criteria for Cr(VI) (50 microg/L). Concentrations of dissolved total Cr in pore water ranged from <2.0 to 5.3 microg/L, while Cr(VI) was not detected (<10 microg/L). These findings are consistent with previous studies, which demonstrated limited bioavailability and toxicity of Cr in sediment at this site and others with similar conditions.

Indirect photolysis of perfluorochemicals: hydroxyl radical-initiated oxidation of N-ethyl perfluorooctane sulfonamido acetate (N-EtFOSAA) and other perfluoroalkanesulfonamides.

Selected perfluorinated surfactants were irradiated in aqueous hydrogen peroxide solutions using artificial sunlight to study transformation under aquatic environmental conditions. Indirect photolysis mediated by hydroxyl radical was observed for N-ethyl perfluorooctane sulfonamidoethanol (N-EtFOSE), N-ethyl perfluorooctane sulfonamido acetate (N-EtFOSAA), N-ethyl perfluorooctane sulfonamide (N-EtFOSA), and perfluorooctane sulfonamide acetate (FOSAA). An upper limitforthe bimolecular reaction rate constant for reaction of *OH and N-EtFOSAA was determined to be (1.7 +/- 0.7) x 10(9) M(-1)s(-1). A proposed reaction pathwayfor degradation of the parent perfluorochemical, N-EtFOSE, to the other perfluoroalkanesulfonamides and perfluorooctanoate (PFOA) was developed and includes oxidation and N-dealkylation steps. As they did not undergo additional degradation, perfluorooctane sulfonamide (FOSA) and PFOA were the final degradation products of hydroxyl radical-initiated oxidation. UV-visible absorption spectra for the perfluorochemicals, showing absorbance in the UV region below the range of natural sunlight are also reported. In sunlit environments, indirect photolysis of perfluorochemicals is likely to be important in the determination of their environmental fate given the slow rates expected for biotransformation and weak sorption. Photolytic conversion of perfluorochemicals into refractory perfluorinated acids, mainly PFOA, could mean that a significant fraction of these compounds will accumulate in the world's oceans.

Perfluorochemicals in water reuse.

Faced with freshwater shortages, water authorities are increasingly utilizing wastewater reclamation to augment supplies. However, concerns over emerging trace contaminants that persist through wastewater treatment need to be addressed to evaluate potential risks. In the present study, perfluorinated surfactant residues were characterized in recycled water from four California wastewater treatment plants that employ tertiary treatment and one that treats primary sewage in a wetland constructed for both treatment and wildlife habitat. Effluent concentrations were compared with surface and groundwater from a creek where recycled water was evaluated as a potential means to augment flow (Upper Silver and Coyote Creeks, San Jose, CA). In the recycled water, 90-470 ng/l perfluorochemicals were detected, predominantly perfluorooctanoate (PFOA; 10-190 ng/l) and perfluorooctanesulfonate (PFOS; 20-190 ng/l). No significant removal of perfluorochemicals was observed in the wetland (total concentration ranged 100-170ng/l across various treatment stages); in this case, 2-(N-ethylperfluorooctanesulfonamido) acetic acid (N-EtFOSAA), perfluorodecanesulfonate (PFDS), and PFOS were dominant. Though there is currently no wastewater discharge into the creeks, perfluorochemicals were found in the surface water and underlying groundwater at a total of 20-150 ng/l with PFOS and PFOA again making the largest contribution. With respect to ecotoxicological effects, perfluorochemical release via recycled water into sensitive ecosystems requires evaluation.