Adsorption and leaching of fluorotelomer compounds and perfluoroalkyl acids in aqueous media by activated carbon prepared from municipal biosolids.

Perfluoroalkyl acids (PFAAs) are ubiquitous in nature and pose serious health risks to humans and animals. Limiting PFAA exposure requires novel technology for their effective removal from water. We investigated the efficacy of biosolid-based activated carbon (Bio-SBAC) in removing frequently detected PFAAs and their precursor fluorotelomer compounds at environmentally relevant concentrations (∼50 µg/L). Batch experiments were performed to investigate adsorption kinetics, isotherms, and leachability. Bio-SBAC achieved >95% removal of fluorotelomeric compounds, indicating that the need for PFAA removal from the environment could be minimised if the precursors were targeted. Kinetic data modelling suggested that chemisorption is the dominant PFAA adsorption mechanism. As evidenced by the isotherm modelling results, Freundlich adsorption intensity, n-1, values of <1 (0.707-0.938) indicate chemisorption. Bio-SBAC showed maximum capacities for the adsorption of perfluorooctanoic acid (1429 µg/g) and perfluorononanoic acid (1111 µg/g). Batch desorption tests with 100 mg/L humic acid and 10 g/L NaCl showed that Bio-SBAC effectively retained the adsorbed PFAA with little or no leaching, except perfluorobutanoic acid. Overall, this study revealed that Bio-SBAC is a value-added material with promising characteristics for PFAA adsorption and no leachability. Additionally, it can be incorporated into biofilters to remove PFAAs from stormwater, presenting a sustainable approach to minimise biosolid disposal and improve the quality of wastewater before discharge into receiving waters.

Removal of perfluoroalkyl acids from aqueous media by surfactant-modified clinoptilolites.

Perfluoroalkyl and polyfluoroalkyl substances (PFASs) are environmentally persistent, bioaccumulating, and toxic compounds that have attracted global attention. It is challenging to reduce the residual concentrations of these compounds to safe discharge limits. In this study, batch experiments were performed to evaluate natural clinoptilolite and clinoptilolites modified (MC) with cetylpyridinium chloride (CPC-MC), didodecyldimethylammonium bromide (DDAB-MC), hexadecyltrimethylammonium bromide (HDTMA-MC), and tetramethylammonium chloride (TMA-MC) as cost-effective aqueous PFAS adsorbents. The removal capacities of the adsorbents for the majority of the PFASs decreased in the following order: DDAB-MC > CPC-MC ≫ modified natural clinoptilolite with hexadecyltrimethyl ammonium bromide (HDTMA-MC) ≫ modified natural clinoptilolite with tetramethylammonium chloride (TMA-MC) ≈ natural clinoptilolite modified with NaCl (NC). In particular, CPC-MC and DDAB-MC reduced PFASs concentration in 50 µg/L by up to 98% for perfluorooctane sulphonate. Within 30 min, CPC-MC (30.5 µg/L) and DDAB-MC (32.1 µg/L) met the PFOS water quality criterion of 36 µg/L in inland surface waters. Both adsorbents met this criterion at the highest solution volume (40 mL) and 0.125 g/L (solid-to-liquid ratio of 1:8). PFASs with short hydrocarbon chains competed more for adsorption. PFASs with sulphonate functional groups were also adsorbed more than carboxyl groups in single- and multi-PFAS solutions. The modified surfaces of clinoptilolites controlled PFAS adsorption through hydrophobic and electrostatic interactions. PFAS removal with surfactant-modified clinoptilolites is cost-effective and protects aquatic environments by using surplus natural materials.

PRL2 Phosphatase Promotes Oncogenic KIT Signaling in Leukemia Cells through Modulating CBL Phosphorylation.

Receptor tyrosine kinase KIT is frequently activated in acute myeloid leukemia (AML). While high PRL2 (PTP4A2) expression is correlated with activation of SCF/KIT signaling in AML, the underlying mechanisms are not fully understood. We discovered that inhibition of PRL2 significantly reduces the burden of oncogenic KIT-driven leukemia and extends leukemic mice survival. PRL2 enhances oncogenic KIT signaling in leukemia cells, promoting their proliferation and survival. We found that PRL2 dephosphorylates CBL at tyrosine 371 and inhibits its activity toward KIT, leading to decreased KIT ubiquitination and enhanced AKT and ERK signaling in leukemia cells. IMPLICATIONS: Our studies uncover a novel mechanism that fine-tunes oncogenic KIT signaling in leukemia cells and will likely identify PRL2 as a novel therapeutic target in AML with KIT mutations.

Co-pyrolysis of sewage sludge and biomass waste into biofuels and biochar: A comprehensive feasibility study using a circular economy approach.

Enormous annual sewage sludge (SS) volumes pose global environmental challenges owing to contamination and significant greenhouse gas emissions. Here, we investigated the economic viability of co-pyrolyzing SS and biomass waste to produce biofuels (bio-oil and gas) and biochar. Net present worth (NPW) analysis, the sale product break-even price, and sludge handling price (SHP) were used to determine the profitability of co-pyrolysis compared with SS pyrolysis alone and conventional treatment methods. In this study, the sale prices of biochar based on quality (i.e., stability, carbon sequestration effectiveness, and heavy metal content) were estimated to be 2.24, 1.44, and 0.98 CAD/kg for high-, medium-, and low-grade biochar. The bio-oil prices, estimated based on the higher heating values of bio-oil and diesel, ranged from 0.80 to 1.22 CAD/kg. Sawdust (SD) and wheat straw (WS) were the chosen co-pyrolysis feedstocks, with four mixing ratios (20, 40, 60, and 80 wt%). Economically, SD (40 wt% mixing ratio) co-pyrolysis achieved the best performance, with a maximum NPW of 8.71 million CAD. SD single and co-pyrolysis were the only profitable scenarios. Moreover, SS single pyrolysis and WS co-pyrolysis exhibited higher profitability than conventional SS treatment methods, with SHPs of 65 and 40 CAD/1000 kg dry sludge, respectively. Sensitivity analysis highlighted the dependence of economic performance on biochar and bio-oil market value. This study offers the first economic analysis of this approach and enhances our understanding of the potential of co-pyrolysis for biofuel and biochar production, providing innovative solutions for the environmental challenges of SS disposal.

Emerging applications of biochar: A review on techno-environmental-economic aspects.

Biomass fast pyrolysis produces bio-oil and biochar achieving circular economy. This review explored the emerging applications of biochar. Biochar possesses the unique properties for removing emerging contaminants and for mine remediation, owing to its negative charge surface, high specific surface area, large pore size distribution and surface functional groups. Additionally, biochar could adsorb impurities such as CO2, moisture, and H2S to upgrade the biogas. Customizing pyrolysis treatments, optimizing the feedstock and pyrolysis operating conditions enhance biochar production and improve its surface properties for the emerging applications. Life cycle assessment and techno-economic assessment indicated the benefits of replacing conventional activated carbon with biochar.

New scaffolds for type II JAK2 inhibitors overcome the acquired G993A resistance mutation.

Recurrent JAK2 alterations are observed in myeloproliferative neoplasms, B-cell acute lymphoblastic leukemia, and other hematologic malignancies. Currently available type I JAK2 inhibitors have limited activity in these diseases. Preclinical data support the improved efficacy of type II JAK2 inhibitors, which lock the kinase in the inactive conformation. By screening small molecule libraries, we identified a lead compound with JAK2 selectivity. We highlight analogs with on-target biochemical and cellular activity and demonstrate in vivo activity using a mouse model of polycythemia vera. We present a co-crystal structure that confirms the type II binding mode of our compounds with the "DFG-out" conformation of the JAK2 activation loop. Finally, we identify a JAK2 G993A mutation that confers resistance to the type II JAK2 inhibitor CHZ868 but not to our analogs. These data provide a template for identifying novel type II kinase inhibitors and inform further development of agents targeting JAK2 that overcome resistance.

A comparative life-cycle assessment and cost analysis of biofilters amended with sludge-based activated carbon and commercial activated carbon for stormwater treatment.

Environmental and economic issues resulting from the unsustainable management of sewage sludge from wastewater have necessitated the development of eco-friendly sewage sludge disposal methods, whereas stormwater effluent contains tremendous amounts of pollutants. This study compares the feasibility and environmental impacts associated with incorporating biofilters with sludge-based activated carbon (SBAC) versus commercial activated carbon (CAC) for stormwater treatment. The results demonstrate that the construction and disposal life-cycle stages are the dominant contributors to several environmental impact categories, including resource scarcity, carcinogenic toxicity, terrestrial ecotoxicity, and ozone formation indicators. Across multiple impact categories, the incorporation of biofilters with SBAC can reduce the negative environmental impacts associated with biofilter construction and disposal by 40% over a 50-year analysis period. In contrast, the most significant improvement is on construction-dominant indicators, where the decreased need for biofilter reconstruction results in a higher reduction in environmental impacts. Economically, amending the biofilter with SBAC can increase profits by up to 66% due to extending its lifespan. This study shows that SBAC has similar performance as CAC for lowering the negative environmental impacts resulting from biofilter construction, while increasing the overall net profits of the system. However, converting sewage sludge to an effective sorbent (SBAC) and incorporating SBAC into a biofilter to capture pollutants from stormwater is an economically and environmentally sustainable solution available to practitioners to manage sewage sludge and stormwater effluent. This solution protects the environment in a cost efficient, sustainable manner.

Using circular economy principles in the optimisation of sludge-based activated carbon production for the removal of perfluoroalkyl substances.

Massive sewage sludge (SS) production from municipal wastewater treatment plants and the presence of numerous pollutant types render the process of SS treatment and disposal costly and complex. Here, resource recovery from SS was maximised via the optimisation of sludge-based activated carbon (SBAC) production for the removal of poly- and perfluoroalkyl substances (PFASs), while considering economic factors and minimising environmental impacts. SBAC production optimisation was realised under different operating conditions (different ZnCl2 impregnation ratios and different pyrolysis activation temperatures and durations). The sorption capacity of the optimised SBAC with respect to the removal of nine commonly detected PFASs, with environmentally relevant concentrations (∽50 µg/L), from simulated wastewater was evaluated. Economic analysis and life-cycle assessment (LCA) were also performed to determine the feasibility of the process and its potential role in the circular economy. Batch adsorption tests confirmed the high efficiency of the optimised SBACs for PFAS removal (93-100 %), highlighting the possibility of converting SS to SBAC. Economically speaking, the optimised SBAC at 1.5 M ZnCl2, 500 °C, and 0.75 h reduced total production cost by 49 %. Further, the cost could be reduced to as little as 1087 US $/metric-ton compared with that corresponding to the original conditions (2.5 M ZnCl2, 500 °C, 2 h; 2144 US $/metric-ton). LCA results also showed that freshwater ecotoxicity, marine ecotoxicity, and human non-carcinogenic toxicity were the most affected environmental impact indicators, showing a 49 % decrease when ZnCl2 impregnation ratio was reduced from 2.5 to 1.5 M. These findings highlighted the optimal conditions for the production of SBAC with high sorption capacity at a reduced cost and with reduced environmental impacts. Thus, they can serve as valuable tools for decision making regarding the selection of the most sustainable and economically feasible process for PFAS removal.

Antibacterial Activity of a Natural Clay Mineral against Burkholderia cepacia Complex and Other Bacterial Pathogens Isolated from People with Cystic Fibrosis.

There is an impending crisis in healthcare brought about by a new era of untreatable infections caused by bacteria resistant to all available antibiotics. Thus, there is an urgent need to identify novel antimicrobial agents to counter the continuing threat posed by formerly treatable infections. We previously reported that a natural mineral clay known as Kisameet clay (KC) is a potent inhibitor of the organisms responsible for acute infections. Chronic bacterial infections present another major challenge to treatment by antimicrobials, due to their prolonged nature, which results in repeated exposure to antibiotics and a constant selection for antimicrobial resistance. A prime example is bacteria belonging to the Burkholderia cepacia complex (Bcc), which particularly causes some of the most serious chronic lung infections in patients with cystic fibrosis (CF) associated with unpredictable clinical outcomes, poor prognosis, and high mortality rates. Eradication of these organisms from CF patients with limited effective antimicrobial options is a major challenge. Novel therapeutic approaches are urgently required. Here, we report the in vitro antibacterial activity of KC aqueous suspensions (1-10% w/v) and its aqueous extract (L100) against a collection of extensively and multi-drug resistant clinical isolates of Bcc, Pseudomonas aeruginosa, and Stenotrophomonas maltophilia isolated from patients with CF. These findings present a potential novel therapy for further investigation in the clinic.

PRL2 phosphatase enhances oncogenic FLT3 signaling via dephosphorylation of the E3 ubiquitin ligase CBL at tyrosine 371.

Acute myeloid leukemia (AML) is an aggressive blood cancer with poor prognosis. FMS-like tyrosine kinase receptor-3 (FLT3) is one of the major oncogenic receptor tyrosine kinases aberrantly activated in AML. Although protein tyrosine phosphatase PRL2 is highly expressed in some subtypes of AML compared with normal human hematopoietic stem and progenitor cells, the mechanisms by which PRL2 promotes leukemogenesis are largely unknown. We discovered that genetic and pharmacological inhibition of PRL2 significantly reduce the burden of FLT3-internal tandem duplications-driven leukemia and extend the survival of leukemic mice. Furthermore, we found that PRL2 enhances oncogenic FLT3 signaling in leukemia cells, promoting their proliferation and survival. Mechanistically, PRL2 dephosphorylates the E3 ubiquitin ligase CBL at tyrosine 371 and attenuates CBL-mediated ubiquitination and degradation of FLT3, leading to enhanced FLT3 signaling in leukemia cells. Thus, our study reveals that PRL2 enhances oncogenic FLT3 signaling in leukemia cells through dephosphorylation of CBL and will likely establish PRL2 as a novel druggable target for AML.

Microplastic removal from urban stormwater: Current treatments and research gaps.

Stormwater is a major contributor to microplastic (MP) pollution in the aquatic environment. Although MPs are associated with many toxicological effects, their levels in stormwater are not regulated. This review compared the effectiveness of different MP removal technologies from stormwater runoff and examined the performance of typical stormwater treatment systems for MP removal to assess possible MP pollution control via stormwater management. Bioretention and filtration systems performed similarly with 84-96% MP removal efficiencies. Despite the limited number of studies that focused on wetlands and retention ponds, preliminary data suggested potential for MP removal with efficiencies of 28-55% and 85-99%, respectively. Despite the higher efficiency of bioretention and filtration systems, their removal efficiency of fibrous MPs was not optimal. Furthermore, wetlands were less effective in removing MPs than retention ponds, although the limited data might lead to an inaccurate representation of typical performances. Therefore, more research is required to arrive at definitive conclusions and to investigate alternative treatment options, such as ballasted sand flocculation, flotation, and biological degradation, and evaluate the effectiveness of bioretention and filtration for MPs <100 µm.

Adsorption of p-benzoquinone at low concentrations from aqueous media using biosolid-based activated carbon.

The toxic oxidation intermediate p-benzoquinone exists in aqueous environments at dilute concentrations above the fish-toxicity limit of 0.045 mg/L, affecting aquatic life. The reduction of this compound to the concentrations required to achieve safe discharge limits is challenging. In this study, the adsorptive removal of p-benzoquinone by a biosolid-based activated carbon (SBAC) was systematically investigated in batch experiments. The adsorption rate was rapid, and the bulk of p-benzoquinone adsorption occurred within 30 min. The maximum adsorption capacity of SBAC was estimated at 19.6 mg/g using the Langmuir isotherm model. Its adsorptivity was independent of temperature from 6 to 40 °C. The presence of 6 g/L of chloride and 500 mg/L of sulphate did not affect the removal of 1 mg/L p-benzoquinone, whereas 15 mg/L of humic acid media slightly decreased the p-benzoquinone removal from 87.0% to 83.2%. Diffusion, hydrophilic, and electrostatic interactions (i.e., dipole-dipole) govern the adsorption of p-benzoquinone and are influenced by the SBAC surface chemistry. Biosolid-based activated carbon can lower the residual p-benzoquinone to below the fish-toxicity limit of 0.045 mg/L within 1 h of sequential adsorption. Thus, biosolid-based activated carbon can effectively remove p-benzoquinone from aqueous environments; this is a waste-to-resource approach that addresses sustainability (waste disposal) and environmental protection (pollutant removal).

Biosolids-based activated carbon for enhanced copper removal from citric-acid-rich aqueous media.

In this study, we employed batch experiments to assess the effects of citric acid on the Cu(II) removal efficiencies of seven biosolids-based adsorbents. The adsorbents used were dried biosolids (BS), biosolids biochar (BSBC), biosolids-based activated carbon (SBAC), nitric-acid-modified BSBC (BSBC-HNO3) and SBAC (SBAC-HNO3), and amine-modified BSBC (BSBC-NH2) and SBAC (SBAC-NH2). However, with 100 mM citric acid in 1 mM Cu(II) solution, only SBAC showed an increase in Cu(II) removal efficiency (64.0-93.5%). Therefore, we used SBAC for further optimisation of the adsorption process. The kinetics data, optimally described by the pseudo-second-order model, indicated that bulk Cu(II) adsorption occurred within 10 min. The highest Cu(II) removal was at pH 3, with the estimated maximum Cu(II) adsorption capacity of SBAC increasing from 0.14 to 0.30 mmol/g, with 100 mM citric acid present. This result clearly indicated the positive effect of citric acid on Cu(II) adsorption. With citric acid present, the Freundlich model optimally fitted the adsorption isotherm data, suggesting adsorption of Cu(II) in multilayers. Further investigation of Cu(II) adsorption in a sequential setup proved that SBAC could lower the residual Cu(II) in the solution to below the discharge limit (0.05 mM) in 1 h. Overall, the production of activated carbon from BS has been proven an efficient Cu(II) adsorbent for Cu-citric-acid-rich aqueous media as a simulation of real wastewaters/leachates, as well as achieving waste-to-resources goals. This is the first study to identify an adsorbent (SBAC) with increased Cu(II) adsorption capacity in the presence of excess citric acid.

The chromosome 21 kinase DYRK1A: emerging roles in cancer biology and potential as a therapeutic target.

Dual-specificity tyrosine phosphorylation-regulated kinase 1 A (DYRK1A) is a serine/threonine kinase that belongs to the DYRK family of proteins, a subgroup of the evolutionarily conserved CMGC protein kinase superfamily. Due to its localization on chromosome 21, the biological significance of DYRK1A was initially characterized in the pathogenesis of Down syndrome (DS) and related neurodegenerative diseases. However, increasing evidence has demonstrated a prominent role in cancer through its ability to regulate biologic processes including cell cycle progression, DNA damage repair, transcription, ubiquitination, tyrosine kinase activity, and cancer stem cell maintenance. DYRK1A has been identified as both an oncogene and tumor suppressor in different models, underscoring the importance of cellular context in its function. Here, we review mechanistic contributions of DYRK1A to cancer biology and its role as a potential therapeutic target.

Sludge-based activated carbon and its application in the removal of perfluoroalkyl substances: A feasible approach towards a circular economy.

This study explores the recovery of resources and energy from sewage sludge through the production of sludge-based activated carbon (SBAC) considering circular economy principles. The SBAC production costs were estimated under three scenarios considering various sludge dewatering/drying schemes to determine the production feasibility and its role in the circular economy. SBAC was tested in the removal of a mixture of nine commonly detected poly- and perfluoroalkyl substances (PFASs) in environmentally relevant concentrations of ∽50 µg/L in comparison to commercially available activated carbon (AC) using 5 mg of sorbent and 5 mL of a nine-PFAS mixture in deionised water. SBAC can be produced at approximately 1.2 US $/kg, which is substantially lower than the average production cost of commercial AC of >3 US $/kg. A net revenue ranging from 2 to 7 US $/kg SBAC was estimated by recycling the produced non-condensable gases and bio-oil to produce energy and selling the SBAC. Batch adsorption tests showed that the PFASs removal of SBAC was superior to that of granular AC and similar to that of powdered AC, reaching >91% to below the detection limit. The kinetics tests revealed that adsorption by SBAC and AC occurred within 15 min. The overall results demonstrate the potential of SBAC as an effective sorbent for PFASs, achieving waste-to-resources circular economy via resource and energy recovery from sewage sludge, eliminating sludge disposal and contaminant-leaching to the environment, and in enhancing the quality of wastewater effluent before discharge.

Exploratory study of removing nutrients from aqueous environments employing a green synthesised nano zero-valent iron.

This study explores the green synthesis of nano zero-valent iron (nZVI) extracted from the peel of selected waste fruits: banana (BP), mango (MP), and pomegranate (GP), for the removal of nutrients from aqueous environments. The extract was prepared by heating de-ionised water at 60°C for 5 min, adding a reducing and a stabilising agent, FeCl3, then stirring with a N2 gas flush solution to form iron nanoparticles, with a final drying step under N2 conditions. Using a variety of characterisation techniques, it was determined that nZVI particles were successfully synthesised via the reduction of iron (III) to iron (0) and stabilised by the presence of phenolic compounds in the extract. The removal of 20 mg/L nutrients from an aqueous solution carried out using the nZVIs resulted in nitrate removal of 92% (nZVI-GP), 88% (nZVI-BP), and 72% (nZVI-MP) within 5 min, whereas ∼98% phosphate was removed by all three nZVIs within 60 min. The aging effect was also tested. Aging the nZVIs for >20 days resulted in less efficient phosphate adsorption after exposure for 250 min; ∼70% phosphate removal was achieved using the nZVIs under these conditions. The mechanisms and pathways of nitrate reduction, including the adsorption of phosphate by nZVI were demonstrated, and discussed. Leachability tests of the phosphate-loaded nZVIs revealed that 10%, 28%, and 48% phosphate was released from the nZVI-GP, nZVI-BP, and nZVI-MP particles, respectively. Using waste fruit is, therefore, a viable and sustainable alternative to the traditional sodium borohydride method to produce nZVIs for environmental application.

Therapy-related myeloid neoplasms resembling juvenile myelomonocytic leukemia: a case series and review of the literature.

Therapy-related myeloid neoplasms (t-MN) are a distinct subgroup of myeloid malignancies with a poor prognosis that include cases of therapy-related myelodysplastic syndrome (t-MDS), therapy-related myeloproliferative neoplasms (t-MPN) and therapy-related acute myeloid leukemia (t-AML). Here, we report a series of patients with clinical features consistent with juvenile myelomonocytic leukemia (JMML), an overlap syndrome of MDS and myeloproliferative neoplasms that developed after treatment for another malignancy.

Adsorption of polycyclic aromatic hydrocarbons by surfactant-modified clinoptilolites for landfill leachate treatment.

The authors report the potential adsorption capacities of three surfactant-modified clinoptilolites (MC)-cetylpyridinium chloride (CPC)-MC, didodecyldimethylammonium bromide (DDAB)-MC, and hexadecyltrimethylammonium bromide (HDTMA)-MC-for the removal of polycyclic aromatic hydrocarbons (PAHs) from aquatic environments and landfill leachate. A liquid-liquid extraction method was used to extract PAHs from water and GC/MS was used to analyse the PAHs. PAH accumulations on CPC-MC, DDAB-MC, and HDTMA-MC were linear over 21 successive batch adsorption tests for anthracene (708, 737, and 750 µg/g), fluoranthene (1355, 1583, and 1303 µg/g), fluorene (973, 1060, and 1147 µg/g), phenanthrene (844, 1057, and 989 µg/g), and pyrene (1343, 1569, and 1269 µg/g). The leachability after 21 successive accumulations was <2% for anthracene, <4% for fluoranthene, <3% for fluorene, <4% for pyrene, and <5% for phenanthrene for each adsorbent. PAH removals from landfill leachate for anthracene, fluoranthene, fluorene, phenanthrene, and pyrene were 97.8%, 98.6%, 95.7%, 97.0%, and 98.5% for CPC-MC and 99.0%, 99.6%, 98.0%, 99.0%, and 99.6% for DDAB-MC, respectively, meeting the fresh water quality standards established by British Columbia and the World Health Organization (WHO) for anthracene, fluoranthene, and fluorene. The molecular weight and molecular structure of PAHs and the hydrophobicity of adsorbents can fundamentally influence the PAH adsorption mechanism based on π-π stacking.

Exploring indirect photolysis of 6:2 fluorotelomer sulfonate in landfill leachate under simulated sunlight: effect of humic acid and nitrate.

Landfill leachate is exposed to sunlight through on- and off-site leachate treatment and disposal to surface water bodies. Very little is known about the potential phototransformation of fluorotelomer compounds in landfill leachates, which can undergo environmental oxidation and produce perfluorocarboxylic acids (PFCAs). This study investigated phototransformation of spiked 6:2 fluorotelomer sulfonate (FTS) (∼ 100 µg/L) in leachate under simulated sunlight, using a metal halide lamp (wavelength, 390 to 750 nm). To understand the effects of nitrate and humic acid (HA), phosphate buffer (pH 7.1) containing nitrate and HA were spiked with 6:2 FTS and irradiated under simulated sunlight for 72 h. Following irradiation, 6:2 FTS and known transformation products (i.e., PFCAs) were quantified in the samples using LC-MS/MS. The results showed that 6:2 FTS was undergoing indirect photolysis in leachate (half-life of ∼ 15 days), suggesting that indirect photolysis of 6:2 FTS is likely a relevant transformation pathway in sunlit aquatic environments. However, the spiked 6:2 FTS did not show any observable decrease in the presence of nitrate and HA over 72 h. Perfluorohexanoic acid (PFHxA) increased in irradiated leachate background samples (without 6:2 FTS spike) suggesting that phototransformation in sunlit leachate could lead to the formation of persistent PFCAs at environmental concentrations of the precursors. Future studies using probe compounds are recommended to better understand the roles of reactive species in phototransformation of 6:2 FTS.