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This study explored the effect stage number and plant type have on ammonia-nitrogen (NH 3 -N) removal kinetics in a two-stage pilot-scale vertical flow constructed wetland (VFCW) system treating landfill leachate. Half of the VFCW columns were planted with Typha latifolia and the other half Scirpus californicus, and half of the columns were loaded with municipal solid waste landfill leachate (diluted to 1 part leachate to 2 parts total) with the effluent from these columns was collected in two separate barrels. The remaining columns were loaded with the effluent collected from the first columns, creating a two-stage VFCW system with four unique pairs to be tested. The leachate used here experienced no prior pre-treatment, and average influent concentrations of NH 3 -N for the first- and second-stage VFCWs were 508 and 321 mg L -1 , respectively- much higher than many other VFCW treatment systems. Some reduction in chemical oxygen demand was observed, as well as generation of nitrate and nitrite, evidence of nitrification. No apparent correlation between aboveground biomass and removal of NH 3 -N was observed. Overall removal efficiency of NH 3 -N through two stages of VFCWs was 53.7% for columns planted with T. latifolia and 58.3% for those planted with S. Californicus. Average NH 3 -N removal efficiencies for the first stage VFCWs were 32.7% and 34.3%, while those in the second stage were 31.3% and 36.5%; no significant difference was observed between the first and second stage, suggesting that stage number does not have a significant effect on the removal efficiency of NH 3 -N in the primary treatment of landfill leachate via VFCWs. However, average mass removal rates of NH 3 -N in the first stage were 166 and 175 mg L -1 d -1 ; the second stage was significantly lower at 99.4 and 112 mg L -1 d -1 , indicating that the first stage removed more pollutants overall., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Elevated per- and polyfluoroalkyl substance (PFAS) concentrations have been reported in municipal solid waste (MSW) landfill leachate with higher levels in wet and warmer subtropical climates. Information about landfill leachate characteristics is much more limited in tropical climates. In this study, 20 landfill leachate samples were collected from three MSW landfills on the tropical island of Puerto Rico and results were compared against landfills nationally and within Florida, USA. The samples collected in Puerto Rico underwent physical-chemical analysis, as well as a quantitative analysis of 92 PFAS. Samples described in this study include discrete leachate types, such as leachate, gas condensate, and leachate which has undergone on-site treatment (e.g., RO treatment, phytoremediation, lagoons). A total of 51 PFAS were detected above quantitation limits, including perfluorohexylphosphonic acid, a perfluoroalkyl acid (PFAA) which has not been reported previously in landfill leachate. ∑PFAS concentrations in this study (mean: 38,000 ng L -1 ), as well as concentrations of individual PFAS, are significantly higher than other reported MSW landfill leachate concentrations. The profiles of leachates collected from on-site treatment systems indicate possible transformation of precursor PFAS as a result of treatment processes - oxidizing conditions, for example, may facilitate aerobic transformation, increase the concentrations of PFAAs, and possibly increase the apparent ∑PFAS concentration. Extreme climate events, including rising temperatures and more frequent hurricanes, have placed additional strain on the solid waste management infrastructure on the island - adding complexity to an already challenging PFAS management issue. As concern grows over PFAS contamination in drinking water, these findings should inform solid waste and leachate management decisions in order to minimize PFAS emissions in island environments., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier Ltd.)

PER: and polyfluoroalkyl substances (PFAS) have been measured in aqueous components within landfills. To date, the majority of these studies have been conducted in Florida. This current study aimed to evaluate PFAS concentrations in aqueous components (leachate, gas condensate, stormwater, and groundwater) from four landfills located outside of Florida, in Pennsylvania, Colorado, and Wisconsin (2 landfills). The Pennsylvania landfill also provided the opportunity to assess a leachate treatment system. Sample analyses were consistent across studies including the measurements of 26 PFAS and physical-chemical parameters. For the four target landfills, average PFAS concentrations were 6,900, 22,000, 280, and 260 ng L -1 in the leachate, gas condensate, stormwater, and groundwater, respectively. These results were not significantly different than those observed for landfills in Florida except for the significantly higher PFAS concentrations in gas condensate compared to leachate. For on-site treatment at the Pennsylvania landfill, results suggest that the membrane biological bioreactor (MBBR) system performed similarly as aeration-based leachate treatment systems at Florida landfills resulting in no significant decreases in ∑ 26 PFAS. Overall, results suggest a general consistency across US regions in PFAS concentrations within different landfill liquid types, with the few differences observed likely influenced by landfill design and local climate. Results confirm that leachate exposed to open air (e.g., in trenches or in treatment systems) have lower proportions of perfluoroalkyl acid precursors relative to leachate collected in enclosed pipe systems. Results also confirm that landfills without bottom liner systems may have relatively higher PFAS levels in adjacent groundwater and that landfills in wetter climates tend to have higher PFAS concentrations in leachate., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Concentrations of 25 inorganic elements were measured in both bulk ash and individual ash components from residuals at three municipal solid waste incineration (MSWI) facilities in the US (two combined ash (CA) and one bottom ash (BA)). Concentrations were assessed based on particle size and component to understand the contribution from each fraction. The results found that among facilities, the finer size fractions contained elevated concentrations of trace elements of concern (As, Pb, Sb) when compared to the coarse fraction, but concentrations varied among facilities depending on the type of ash and differences in advanced metals recovery processes. This study focused on several constituents of potential concern, As, Ba, Cu, Pb, and Sb, and found that the main components of MSWI ash (glass, ceramic, concrete, and slag) are sources of these elements in the ash streams. For many elements, concentrations were significantly higher in CA bulk and component fractions opposed to BA streams. An acid treatment procedure and scanning electron microscopy/energy-dispersive x-ray spectroscopy analysis revealed that some elements, such as As in concrete, are result of the inherent properties of the component, but other elements, such as Sb, form on the surface during or after incineration and can be removed. Some Pb and Cu concentrations were attributed to inclusions in the glass or slag introduced into the material during the incineration process. Understanding the contributions of each ash component provides critical information for developing strategies to reduce trace element concentrations in ash streams to promote reuse opportunities., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: All Authors report financial support was provided by Hinkley Center for Solid and Hazardous Waste Management., (Copyright © 2023. Published by Elsevier Ltd.)

The environmental risks associated with the storage, reuse, and disposal of unencapsulated reclaimed asphalt pavement (RAP) has been previously examined, but because of a lack of standardized column testing protocols and recent interest on emerging constituents with higher toxicity, questions surrounding leaching risks from RAP continue. To address these concerns, RAP from six, discrete stockpiles in Florida was collected and leach tested following the most up-to-date, standard column leaching protocol - United States Environmental Protection Agency (US EPA) Leaching Environmental Assessment Framework (LEAF) Method 1314. Sixteen EPA priority polycyclic aromatic hydrocarbons (PAHs), 23 emerging PAHs, identified through relevance in literature, and heavy metals were investigated. Column testing showed minimal leaching of PAHs; only eight compounds, three priority PAHs and five emerging PAHs, were released at quantifiable concentrations, and where applicable, were below US EPA Regional Screening Levels (RSL). Though emerging PAHs were identified more frequently, in most cases, priority compounds dominated contributions to overall PAH concentration and benzo(a)pyrene (BaP) equivalent toxicity. Except for arsenic, molybdenum, and vanadium in two samples, metals were found below limits of detection (LOD) or below risk thresholds. Arsenic and molybdenum concentrations diminished over time with increased exposure to liquid, but elevated vanadium concentrations persisted in one sample. Further batch testing linked vanadium to the aggregate component of the sample, unlikely to be encountered in typical RAP sources. As demonstrated by generally low constituent mobility observed during testing, the leaching risks associated with the beneficial reuse of RAP are limited, and under typical reuse conditions, factors of dilution and attenuation would likely reduce leached concentrations below relevant risk-based thresholds at a point of compliance. When considering emerging PAHs with higher toxicities, analyses indicated minimal impact to overall leachate toxicity, further suggesting that with proper management, this heavily recycled waste stream is unlikely to pose leaching risk., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Variable chemistries of liquids from landfills can potentially impact levels of per- and polyfluoroalkyl substances (PFAS). The objective of the current study was to evaluate relationships between physical-chemical properties (bulk measurements, oxygen demand components, and metals) and PFAS concentrations in different types of aqueous landfill samples. Aqueous landfill samples were collected from 39 landfill facilities in Florida, United States. These samples included leachates from landfills that receive different waste types, such as municipal solid waste incineration ash (MSWA), construction and demolition debris (C&D), and municipal solid waste (MSW). Additional aqueous landfill samples were sourced from treated landfill leachate, gas condensate, stormwater, and groundwater from within and near the landfill boundaries. Results showed significant correlations (p < 0.05) between ∑ 26 PFAS and alkalinity (r s  = 0.83), total organic carbon (TOC) (r s  = 0.84), and ammonia (r s  = 0.79) for all leachate types. Other physical-chemical parameters that were significantly correlated (r s  > 0.60, p < 0.05) with PFAS included specific conductivity, chemical oxygen demand (COD), and to a lesser extent, total dissolved solids (TDS) and total solids (TS). For gas condensates, PFAS was significantly correlated with TOC. Stormwater and groundwater, within and near the landfill boundaries, had considerably lower levels of PFAS and had a minimal correlation between PFAS and physical-chemical parameters. Although PFAS concentrations and physical-chemical parameters and their correlations varied between different types of aqueous landfill samples, results suggest that physical-chemical properties can be useful indicators of relative PFAS concentrations within a leachate type. More research is needed to validate the mechanisms that relate physical-chemical parameters to PFAS concentrations in landfill leachates., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Per- and polyfluoroalkyl substances (PFAS) are ubiquitously present in our indoor living environments. Dust is thought to accumulate PFAS released indoors and serve as an exposure pathway for humans. Here, we investigated whether spent air conditioning (AC) filters can be exploited as opportunistic samplers of airborne dust for assessing PFAS burden in indoor environments. Used AC filters from campus facilities (n = 19) and homes (n = 11) were analyzed for 92 PFAS via targeted ultra-high pressure liquid chromatography - tandem mass spectrometry (UHPLC-MS/MS). While 27 PFAS were measured (in at least one filter), the predominant species were polyfluorinated dialkylated phosphate esters (diPAPs), with the sum of 6:2-, 8:2-, and 6:2/8:2diPAPs accounting for approximately 95 and 98 percent of ∑ 27 PFAS in campus and household filters, respectively. Exploratory screening of a subset of the filters revealed the presence of additional species of mono-, di-, and tri-PAPs. Considering the constant human exposure to dust indoors and the potential of PAPs to degrade into terminal species with well-established toxicological risks, assessing dust for these precursor PFAS warrants further investigation with respect to both human health and PFAS loading to landfills from this under studied waste stream., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Per- and polyfluoroalkyl substances (PFAS), found in many consumer products, are commonly disposed of in landfills at the end of their service lives. To identify landfill liquids that should be prioritized for treatment, this study aimed to evaluate PFAS levels in different aqueous samples from landfills and identify relationships between PFAS and landfill characteristics. Twenty-six PFAS including 11 perfluoroalkyl carboxylic acids (PFCAs), 7 perfluoroalkyl sulfonates (PFSAs), and 8 perfluoroalkyl acid precursors (PFAA-precursors) were measured in municipal solid waste (MSW) leachate, construction and demolition debris (CDD) leachate, municipal solid waste incineration (MSWI) ash leachate, gas condensate, stormwater, and groundwater from landfills. Based on the median, results show that PFAS levels in MSW leachate were the highest (10,000 ng L -1 ), CDD leachate were intermediate (6200 ng L -1 ), and MSWI ash leachate were the lowest (1300 ng L -1 ) among the leachates evaluated. PFAS levels in gas condensate (7000 ng L -1 ) were similar to MSW leachate. PFAS in stormwater and groundwater were low (medians were less than 500 ng L -1 ). Dominant subgroups included PFCAs and PFAA-precursors in all leachates. PFSAs were also found in CDD leachate, PFAA-precursors in gas condensate, and PFCAs in stormwater and groundwater. Landfill characteristics significantly correlated with ∑ 26 PFAS included waste proportions (percentage of MSWI ash in landfill, |r s | = 0.22), operational status (active or not, |r s | = 0.27) and rainfall (30-d cumulative rainfall, |r s | = 0.39). The results from this study can be used to prioritize which landfills and which reservoir of liquids (and corresponding subgroup of PFAS) to target for PFAS management., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Antimony is used extensively in consumer goods, including single use plastic bottles, electronics, textiles and automobile brakes, which are disposed of in landfills at the end of their service lives. As a result, Sb is a constituent of concern in landfill emissions. Previous research has focused on leachate (liquid) and waste incineration flue gas emissions; however, Sb has the potential to volatilize through chemical and microbial processes within a landfill. In this study, iron-amended granular activated carbon was used to adsorb volatile metals directly from gas in a full-scale landfill gas collection system. Metals were quantified using acid digestion and ICP-AES analysis. Antimony concentrations far exceeded those previously reported, at up to 733 μg m -3 (mean: 254 μg m -3 ). In addition to Sb, As was also measured at high levels compared to previous research, as high as 740 μg m -3 (mean: 178 μg m -3 ). Using US EPA landfill and landfill gas databases, total Sb emissions via landfill gas are estimated to be approximately 27.3 kg day -1 in the US. Based on other estimates of national and global Sb emissions, this corresponds to approximately 4.5% of total US atmospheric emissions of Sb and 0.42% of global atmospheric emissions. Sb mass release via landfill gas is approximately 3.9 times higher than via leachate emissions. Although gas emissions are higher than expected, the vast majority (99.9%) of Sb present in landfilled MSW remains within the waste mass indefinitely. In addition to these mass release estimates, this experiment suggests that iron-amended activated carbon may offer significant metals removal from LFG, especially in the first months of new well operation., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Trace metals concentrations of 25 elements were determined for 22 subcomponents of biodegradable and non-biodegradable waste samples representing the United States municipal solid waste (MSW) stream collected during three separate waste sorts. The subcomponent trace metal concentrations and estimated composition results were used to predict trace metal concentrations present in the overall MSW stream along with MSW compost and waste to energy (WTE) ash, which were compared to health-based standards (i.e., US EPA regional screening levels) and to values previously reported in the literature. These estimates for potentially problematic elements like As and Sb could be attributed to abundant base materials in MSW, while other elements, such as Pb, were calculated at much lower concentrations than other published studies. This suggests that trace metals measured in actual MSW compost and WTE ash could originate not only from MSW base components but also from other sources, such as highly concentrated low-mass wastes (e.g., e-waste). While the removal of small quantity components with high metal concentrations may reduce concentrations of some potentially problematic metals (e.g., Pb), others (e.g., As and Sb) are likely to persist in quantities that impede reuse and recycling since they are present in the more abundant base MSW components (e.g., papers, plastics, organics). Promoting meaningful reductions in potentially problematic trace metals in MSW-derived materials may require reevaluating their presence in higher-volume, lower-concentrated MSW components such as paper, plastics, and organics., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

Ash products from coal and municipal solid waste combustion constitute a waste stream with characteristics that, unless recycled, require specific disposal practices. Although traditional disposal involves ash placement in a cell dedicated solely for the ash (monofill), new regulations for the management of coal combustion residues in the US might lead to more co-disposal of these residues with unburned municipal solid waste (MSW) that has not been combusted or otherwise processed. Both monofill and co-disposal practices are currently utilized for MSW incineration ash in the US. Column tests were performed using landfill leachate as a leaching solution to simulate co-disposal conditions of ash with MSW, while DI water was used to simulate monofilling. Mobility of As, B and V from coal fly ash was enhanced in the presence of landfill leachate in both batch and column tests, and a similar trend was observed for Cd and Mo release from MSW incineration ash. For several elements, release was greater with the column procedure relative to the batch procedure. The results suggest that long-term implications of co-disposal should be factored into decisions regarding which disposal scenario to pursue., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020. Published by Elsevier Ltd.)

The fate of antimony (Sb) leached from electronic and electrical equipment plastic when disposed of in a municipal solid waste (MSW) landfill was assessed using simulated anaerobic landfill lysimeters and three different batch leaching tests: toxicity characteristic leaching procedure (TCLP), EPA method 1313, and MSW leachate extractions. Plastic from cathode ray tube televisions sets was noted to have the highest Sb concentrations, and was thus the focus of the study. Sb leachability from EPA 1313 stat and TCLP were similar at approximately 0.1% by weight at the same pH (4.93), while MSW landfill leachates extracted less Sb at approximately 0.02% by weight. Solution pH was not the controlling factor, and other conditions resulting from the landfill leachate resulted in lower concentrations of leached Sb. In simulated landfill experiments, Sb leached at approximately 0.01% by weight after a liquid-to-solid ratio of 3. Sb behaves differently in the landfill environment than arsenic leaching from a similar study, most likely from the reducing conditions brought on by the decomposing waste., (Copyright © 2019. Published by Elsevier Ltd.)

Stabilized landfill leachate is characterized by a high concentration of non-biodegradable organic matter, which is similar in chemistry to dissolved organic matter (DOM) in the natural aquatic environment. Magnetic ion exchange (MIEX) resin treatment is well-studied in drinking water for removal of DOM from natural waters. There are fewer studies evaluating MIEX treatment of waste waters, and there is no previous work evaluating MIEX treatment of landfill leachate. This work systematically evaluated MIEX treatment of stabilized landfill leachate and evaluated the results in the context of previous studies of MIEX treatment of natural and waste waters. Five leachates from four landfills were evaluated as a function of MIEX resin dose, mixing time, and regeneration efficiency. MIEX resin removed DOM from landfill leachate, even in the presence of a reported high background concentration of inorganic ions. MIEX resin that was exhausted with leachate DOM was effectively regenerated with a concentrated NaCl solution, and regenerated MIEX resin performed similarly to virgin resin. For a majority of the leachates, the removal trend for MIEX resin was color>UV-absorbing substances>dissolved organic carbon≈COD>total nitrogen. Finally, MIEX resin removed a wider range of DOM from leachate than coagulation. The most important contribution of this work is that MIEX treatment of leachate followed very similar trends as MIEX treatment of natural waters, which will allow previous MIEX data to be used to estimate the treatment efficiency of other waste waters., (Copyright © 2011 Elsevier Ltd. All rights reserved.)

This work spans landfill characteristics, leachate organic matter properties, and coagulation chemistry to provide new insights into the physical-chemical treatability of stabilized landfill leachate. Furthermore, leachate organic matter is viewed in terms of dissolved organic matter (DOM) present in the natural environment, and coagulation chemistry is evaluated based on previous leachate and water treatment coagulation studies. Stabilized leachate was collected from four landfills for a total of seven leachate samples, and samples were coagulated using ferric chloride, ferric sulfate, and aluminum sulfate. Landfill characteristics, such as age, leachate recirculation, and cover material, influenced properties of DOM present in the leachate, as measured by specific ultraviolet (UV) absorbance at 254 nm (SUVA254) and fluorescence excitation-emission matrices. The coagulation performance of the metal salts was ferric sulfate>aluminum sulfate>ferric chloride, and DOM removal followed the trend of color>UV254>dissolved organic carbon>chemical oxygen demand (COD). Finally, a strong association was found between increasing SUVA254 and increasing DOM removal for coagulation of both leachate and natural surface water. Thus, SUVA254 is expected to be a better predictor of leachate treatability, in particular DOM removal, than the traditionally used ratio of biochemical oxygen demand to COD., (Copyright © 2010 Elsevier Ltd. All rights reserved.)