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Onsite non-potable reuse of greywater reduces the energy costs associated with the transport of wastewater and the stress on traditional source waters. However, greywater contains trace organic contaminants (TOrCs) that can be harmful to the aquatic environment when released via irrigation. In this work, the risk associated with TOrCs was evaluated for two potential irrigation scenarios, the use of untreated greywater and the use of greywater treated via conventional activated sludge. Risk quotient (RQ) ratios were calculated using the maximum concentration of each compound in the untreated or treated greywater divided by the relevant aquatic predicted no effect concentration. The TOrCs with RQs > 0.1 or 1 were classified as moderate and high priority, respectively. A review of greywater literature showed that a total of 350 compounds have been detected, with 132 classified as moderate or high priority in untreated greywater. Post-treatment 44 TOrCs remained as high priority due to high concentrations in greywater and/or poor removal during treatment, but only 14 of them were detected in multiple geographic locations. The final list of 14 TOrCs includes plasticizers/flame retardants (di-(2-ethylhexyl) phthalate, bisphenol A, and triphenyl phosphate), surfactants/preservatives/fragrances (4-nonylphenol, benzyldimethyl dodecylammonium chloride, tonalide, methylparaben, and 2-6-di-tert-butyl-4-methylphenol), UV-filters (benzophenone-3 and octocrylene), and pharmaceuticals/antibiotics (acetaminophen, trimethoprim, caffeine, and triclosan). This subset of TOrCs would be useful surrogates to monitor during greywater treatment for irrigation as potential hazards for nearby aquatic environments., (Copyright © 2021. Published by Elsevier Ltd.)

To verify whether cyanobacteria can travel from eutrophic lakes into the surrounding groundwater, a large-scale field investigation, laboratorial incubations, and quartz column penetration tests were carried out in Lake Taihu (China). High-throughput sequencing of 16S rRNA gene amplicons indicated that cyanobacteria operational taxonomic units (OTUs) were present at fifteen out of forty total wells in four cardinal directions at varying distances from the shore of Lake Taihu, up to a maximum of forty-three kilometers. Six cyanobacteria genera were detected including Microcystis, Dolichospermum, Phormidium, Leptolyngbya, Pseudanabaena and Synechococcus. The proportions of Phormidium, Microcystis and Synechococcus OTUs in the total cyanobacterial community were 45.2%, 32.2% and 19.4%, respectively. The qRT-PCR results showed that cyanobacterial abundance decreased with increasing distance from the shore of Lake Taihu. Based on the microscopic analysis of cultures inoculated with groundwater, we found Microcystis, Dolichospermum and Phormidium. Five cyanobacterial genera were able to penetrate columns filled with quartz particles ranging from 100∼200 μm. Finer layers of quartz sands were found to be impenetrable. The rating of infiltration capabilities was Microcystis > Synechococcus > Nostoc > Phormidium > Cylindrospermopsis. Deficient concentrations of microcystins were found (< 1 µg L -1 ) in the groundwater samples. Based on the consideration of different factors (cyanobacterial composition in Lake Taihu, peripheral groundwater, and algal soil crusts), it was deduced that Microcystis likely originated from the lake. Still, Phormidium was probably originated from the soil infiltration. These results suggest that cyanobacteria and their toxins could travel in the groundwater, but this is a size-dependent mechanism., (Copyright © 2021. Published by Elsevier Ltd.)

As potable reuse guidelines and regulations continue to develop, the presence of N-nitrosamines is a primary concern because of their associated health concerns. In this study, bench-, pilot-, and full-scale tests were conducted to focus on the occurrence and treatment of N-nitrosomorpholine (NMOR) in United States (U.S.) potable reuse systems. Out of twelve U.S. wastewater effluents collected, ambient NMOR was detected in eleven (average = 20 ± 18 ng/L); in contrast, only two of the thirteen surface water and stormwater samples had NMOR. Across all of these samples maximum formation potential by chloramination produced an average increase of 3.6 ± 1.8 ng/L. This result underscores the need to understand the sources of NMOR as it is not likely a disinfection byproduct and it is not known to be commercially produced within the U.S. At the pilot-scale, three potable reuse systems were evaluated for ambient NMOR with oxidation (i.e., chlorination and ozonation), biofiltration, and granular activated carbon (GAC). Both pre-oxidation and biofiltration were ineffective at mitigating NMOR during long-term pilot plant operation (at least eight-months). GAC adsorbers were the only pilot-scale treatment to remove NMOR; however, complete breakthrough occurred rapidly from <2000 to 10,000 bed volumes. For comparison, a full-scale reverse osmosis (RO) potable reuse system was monitored for a year and confirmed that RO effectively removes NMOR. Systematic bench-scale UV-advanced oxidation experiments were undertaken to assess the mitigation potential for NMOR. At a fluence dose of 325 ± 10 mJ/cm 2 , UV alone degraded 90% of the NMOR present. The addition of 5 mg/L hydrogen peroxide did not significantly decrease the UV dose required for one-log removal. These data illustrate that efficient NMOR removal from potable reuse systems is limited to RO or UV treatment., (Copyright © 2018 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Perfluoroalkyl and polyfluoroalkyl substances (PFASs) are a group of persistent contaminants that have been identified throughout the aquatic environment. In this study, ten targeted perfluoroalkyl acids (PFAAs), three targeted PFAA precursors, and non-targeted PFAA precursors were monitored in four full- and pilot-scale potable reuse plants at each stage of advanced treatment. Non-targeted PFAA precursors were quantified by applying a total oxidizable precursor assay in which PFAA precursors are oxidized by hydroxyl radicals to targeted PFAAs. Two of the potable reuse systems had membrane-based treatments with reverse osmosis and UV-advanced oxidation (RO-UV/AOP) and two used ozone, biological activated carbon filtration and granular activated carbon adsorption (O 3 -BAC-GAC). The total targeted PFAAs in the four tertiary effluents, the influent sources for the potable reuse systems, ranged from 52 to 227 ng/L with non-targeted PFAA precursors accounting for 30-67% of total PFASs on a molar basis. The RO-UV/AOP treatment trains reduced PFAAs and PFAA precursors to below their method reporting limits through the barrier provided by RO. The O 3 -BAC-GAC based treatment trains reduced, but did not completely remove PFAAs or PFAA precursors and the PFASs present in the product water were primarily shorter-chain PFAAs, some of which lack human health guidance values for drinking water. The relative fraction of targeted shorter-chain PFAAs increased after each treatment step indicating that there was preferential removal of the PFAA precursors and longer-chain PFAAs. This study provides new insight on the concentrations and treatment of PFAA precursors through potable reuse treatment systems., (Copyright © 2018 Elsevier Ltd. All rights reserved.)