Compound-Specific Carbon, Nitrogen, and Hydrogen Isotope Analysis to Characterize Aerobic Biodegradation of 2,3-Dichloroaniline by a Mixed Enrichment Culture.

Compound-specific isotope analysis (CSIA) is an established tool to track the in situ transformation of organic chemicals at contaminated sites. In this work, we evaluated the potential of multi-element CSIA to assess biodegradation of 2,3-dichloroaniline (2,3-DCA), which is a major industrial feedstock. Using controlled laboratory experiments, we determined, for the first time, negligible carbon (<0.5‰) and hydrogen (<10‰) isotope fractionation and a significant inverse nitrogen isotope fractionation (>10‰) during aerobic 2,3-DCA biodegradation by a mixed enrichment culture. The tentative identification of a glutamate conjugate of 2,3-DCA as a reaction intermediate indicates that the initial multistep enzymatic reaction may be rate-limiting. The formation of the glutamate adduct would increase the bond energy at the N atom, thus likely explaining the observed inverse N isotope fractionation. The corresponding nitrogen enrichment factor was +6.8 ± 0.6‰. This value was applied to investigate the in situ 2,3-DCA biodegradation at a contaminated site where the carbon and nitrogen isotope signatures from field samples suggested similar aerobic processes by native microorganisms. Under the assumption of the applicability of the Rayleigh model in a pilot wetland treating contaminated groundwater, the extent of biodegradation was estimated to be up to 80-90%. This study proposes multi-element CSIA as a novel application to study 2,3-DCA fate in groundwater and surface water and provides insights into biodegradation pathways.

Compound-Specific Carbon, Hydrogen, and Nitrogen Isotope Analysis of Nitro- and Amino-Substituted Chlorobenzenes in Complex Aqueous Matrices.

Compound-specific isotope analysis (CSIA) is an established tool to study the fate of legacy groundwater contaminants but is only emerging for nonconventional contaminants, e.g., nitro- and amino-substituted chlorobenzenes that are widely used as industrial feedstock and the target of this work. To date, CSIA of the target compound groups used special combustion interfaces and the potential matrix interferences in environmental samples has not been assessed. We validated CSIA methods for δ13C, δ2H, and δ15N of four analytes from each chemical group and developed a solid-phase extraction (SPE) method to minimize matrix interferences during preconcentration of complex aqueous samples. The SPE recovery was >80% and the method quantification limits of SPE-CSIA for δ13C, δ2H, and δ15N were 0.03-0.57, 1.3-2.7, and 3.4-10.2 µM aqueous-phase concentrations, respectively, using 2 L of spiked MQ water. The SPE-CSIA procedure showed negligible isotope fractionation for δ13C (≤0.5‰), δ15N (≤0.5‰), and δ2H (≤5‰ for nitroaromatics and ≤10‰ for aminoaromatics). In addition, solvent evaporation, water sample storage up to 7 months, and SPE extract storage for 1.5 years did not change analytes' δ13C signatures beyond ±0.5‰. However, to avoid significant δ2H and δ15N fractionation of aminoaromatics, cartridge breakthrough should be avoided and SPE preconcentration must be conducted at pH > pKa + 2. Application of the method at a contaminated site showed excellent precision, at ≤0.3‰ for C and N, and ≤1.5‰ for H. The methods validated here now allow the use of multielement CSIA to track the environmental fate of nitro- and amino-substituted chlorobenzenes in complex aqueous samples.

Is In-Service Granular Activated Carbon Biologically Active? An Evaluation of Alternative Experimental Methods to Distinguish Adsorption and Biodegradation in GAC.

In-service granular activated carbon (GAC) may transform into biological activated carbon (BAC) and remove contaminants through both adsorption and biodegradation, but it is difficult to determine its biodegradative capacity. One approach to understand the GAC biodegradative capacity is to compare the performance between unsterilized and sterilized GAC, but the sterilization methods may not ensure effective microbial inhibition and may affect adsorption. This study identified the 14C-glucose respiration rate as the best metric to evaluate the effectiveness of three sterilization methods: sodium azide addition, autoclaving, and γ irradiation. The sterilization protocols were refined, including continuously feeding 300 mg/L of sodium azide, three cycles of autoclaving, and 10-12 kGy of γ irradiation. Parallel minicolumn tests were conducted to identify sodium azide addition as the most broadly effective sterilization method with an insignificant effect on adsorption in most cases, except for the adsorption of anionic compounds under certain conditions. Nevertheless, this problem was solved by decreasing the azide dosage as long as it is still sufficient to provide effective microbial inhibition. This study helps to develop an approach that differentiates adsorption and biodegradation in GAC, which could be used by future studies to advance our understanding of BAC filtration.

Stormwater Bioretention Cells Are Not an Effective Treatment for Persistent and Mobile Organic Compounds (PMOCs).

Bioretention cells are a stormwater management technology intended to reduce the quantity of water entering receiving bodies. They are also used to reduce contaminant releases, but their performance is unclear for hydrophilic persistent and mobile organic compounds (PMOCs). We developed a novel eight-compartment one-dimensional (1D) multimedia model of a bioretention cell ("Bioretention Blues") and applied it to a spike and recovery experiment conducted on a system near Toronto, Canada, involving PMOC benzotriazole and four organophosphate esters (OPEs). Compounds with (log DOC) (organic carbon-water distribution coefficients) < ∼2.7 advected through the system, resulting in infiltration or underdrain flow. Compounds with log DOC > 3.8 were mostly sorbed to the soil, where subsequent fate depended on transformation. For compounds with 2.7 ≤ log DOC ≤ 3.8, sorption was sensitive to event size and compound-specific diffusion parameters, with more sorption expected for smaller rain events and for compounds with larger diffusion coefficients. Volatilization losses were minimal for all compounds tested. Direct uptake by vegetation also played a negligible role regardless of the compounds' physicochemical properties. Nonetheless, model simulations showed that vegetation could play a role by increasing transpiration, thereby increasing sorption to the bioretention soil and reducing PMOC release. Model results suggest design modifications to bioretention cells.

Trace Organic Contaminant Transfer and Transformation in Bioretention Cells: A Field Tracer Test with Benzotriazole.

Bioretention cells can effectively infiltrate stormwater runoff and partly remove conventional water contaminants. A field tracer injection experiment in a conventionally designed bioretention cell was used to investigate the fate of benzotriazole, a model trace organic contaminant, during and between runoff events. Moderate (29%) benzotriazole load reductions were measured during the 6 h long injection experiment. The detection of 1-methyl benzotriazole, hydroxy benzotriazole, and methoxy benzotriazole provided in situ evidence of some rapid benzotriazole microbial transformation during the tracer test and more importantly between the events. The detection of benzotriazole alanine and benzotriazole acetyl alanine also showed fast benzotriazole phytotransformation to amino acid conjugates during the tracer test and suggests further transformation of phytotransformation products between events. These data provide conclusive full-scale evidence of benzotriazole microbial and phytotransformation in bioretention cells. Non-target chemical analysis revealed the presence of a diverse range of trace organic contaminants in urban runoff and exiting the bioretention cell, including pesticides and industrial, household, and pharmaceutical compounds. We have demonstrated the in situ potential of urban green infrastructure such as bioretention cells to eliminate polar trace organic contaminants from stormwater. However, targeted design and operation strategies, for example, hydraulic control and the use of soil amendments, should be incorporated for improved bioretention cell performance for such compounds.

Resilience to multiple stressors in an aquatic plant and its microbiome.

PREMISE: Outcomes of species interactions, especially mutualisms, are notoriously dependent on environmental context, and environments are changing rapidly. Studies have investigated how mutualisms respond to or ameliorate anthropogenic environmental changes, but most have focused on nutrient pollution or climate change and tested stressors one at a time. Relatively little is known about how mutualisms may be altered by or buffer the effects of multiple chemical contaminants, which differ fundamentally from nutrient or climate stressors and are especially widespread in aquatic habitats. METHODS: We investigated the impacts of two contaminants on interactions between the duckweed Lemna minor and its microbiome. Sodium chloride (salt) and benzotriazole (a corrosion inhibitor) often co-occur in runoff to water bodies where duckweeds reside. We tested three L. minor genotypes with and without the culturable portion of their microbiome across field-realistic gradients of salt (3 levels) and benzotriazole (4 levels) in a fully factorial experiment (24 treatments, tested on each genotype) and measured plant and microbial growth. RESULTS: Stressors had conditional effects. Salt decreased both plant and microbial growth and decreased plant survival more as benzotriazole concentrations increased. In contrast, benzotriazole did not affect microbial abundance and even benefited plants when salt and microbes were absent, perhaps due to biotransformation into growth-promoting compounds. Microbes did not ameliorate duckweed stressors; microbial inoculation increased plant growth, but not at high salt concentrations. CONCLUSIONS: Our results suggest that multiple stressors matter when predicting responses of mutualisms to global change and that beneficial microbes may not always buffer hosts against stress.

Optimizing Constructed Wetlands for Safe Removal of Triclosan: A Box-Behnken Approach.

Traditional constructed wetland designs typically result in variable efficiencies for trace organic contaminant removal. In this work, we used a Box-Behnken experimental design for optimizing the conditions of pH, nitrate concentration, and dissolved organic carbon (DOC) concentration that would maximize the rate of triclosan phototransformation while minimizing the accumulation of toxic byproducts. Triclosan is a frequently detected and toxic antimicrobial agent present in many consumer and industrial products. The results showed that high pH values (9.9) and low DOC concentration (11 mg/L-) would maximize triclosan phototransformation rate while minimizing the accumulation of toxic byproducts. As long as DOC concentrations were larger than 33 mg/L, nitrate concentration did not show a significant effect on triclosan phototransformation rate. The major transformation products detected were 2,4-dichlorophenol and compounds with chemical formulas C12H8Cl2O2 and C12H9ClO3, resulting from a chlorine loss or replacement by a OH group. In addition, 4-chlorocatechol was mainly detected during direct photolysis and 2,8-dichlorodibenzo-p-dioxin was only found during direct photolysis at pH 8. This study showed that wetland efficiency at removing triclosan can theoretically be increased by limiting DOC-contributing factors, e.g., emergent vegetation, and supporting pH-increase processes, e.g., via algae growth or by incorporating alkaline geomedia.

Biogeochemical Controls on Strontium Fate at the Sediment-Water Interface of Two Groundwater-Fed Wetlands with Contrasting Hydrologic Regimes.

Radioactive strontium (Sr) is a common groundwater contaminant at many nuclear sites. Its natural retention in groundwater-fed wetlands is an attractive remediation strategy. However, at present, the biogeochemical mechanisms controlling Sr transport at the sediment-water interface are poorly understood. In this field study, Sr fate was investigated in two wetlands with contrasting vegetation and hydrologic regimes. The marsh was an open-water wetland with constant water table and no emergent vegetation. The swamp was vegetated with fluctuating water levels and a thick mat of submerged cattail litter in the water column. High-resolution porewater Sr concentrations and solid-phase sediment Sr species revealed distinct profiles between the two wetlands. The marsh exhibited a strongly reduced environment and sharp concentration peaks at the sediment-water interface. In contrast, the smaller concentration gradients of the swamp resulted in a reduced flux of Sr to the surface water. The organic fraction of the sediment dominated Sr retention compared to the inorganic iron and manganese oxides. However, the marsh had a significant fraction of recalcitrant Sr presumably due to its incorporation into sulfur and/or carbonate minerals. These results suggest that vegetated wetlands with fluctuating hydrologic regimes could act as efficient sinks for Sr pollution.

Sediment Monitored Natural Recovery Evidenced by Compound Specific Isotope Analysis and High-Resolution Pore Water Sampling.

Monitoring natural recovery of contaminated sediments requires the use of techniques that can provide definitive evidence of in situ contaminant degradation. In this study, a passive diffusion sampler, called "peeper", was combined with Compound Specific Isotope Analysis to determine benzene and monochlorobenzene (MCB) stable carbon isotope values at a fine vertical resolution (3 cm) across the sediment water interface at a contaminated site. Results indicated significant decrease in concentrations of MCB from the bottom to the top layers of the sediment over 25 cm, and a 3.5 ‰ enrichment in δ13C values of MCB over that distance. Benzene was always at lower concentrations than MCB, with consistently more depleted δ13C values than MCB. The redox conditions were dominated by iron reduction along most of the sediment profile. These results provide multiple lines of evidence for in situ reductive dechlorination of MCB to benzene. Stable isotope analysis of contaminants in pore water is a valuable method to demonstrate in situ natural recovery of contaminated sediments. This novel high-resolution approach is critical to deciphering the combined effects of parent contaminant (e.g., MCB) degradation and both production and simultaneous degradation of daughter products, especially benzene.

Compound specific isotope analysis of hexachlorocyclohexane isomers: a method for source fingerprinting and field investigation of in situ biodegradation.

RATIONALE: The manufacturing and uses of hexachlorocyclohexane (HCH) have resulted in a serious environmental challenge and legacy. This study highlights the ability of compound specific isotope analysis (CSIA) to distinguish among various HCH sources and to support the evaluation of the potential for in situ biodegradation in contaminated groundwater. METHODS: Tests were conducted to verify the absence of significant isotope fractionation during HCH sample pre-concentration including dichloromethane extraction, solvent exchange into iso-octane, and H2SO4 clean-up, and analysis by gas chromatography/combustion-isotope ratio mass spectrometry (GC/C-IRMS). The method was then applied to four Technical Grade (TG) HCH mixtures procured from different sources and to groundwater samples from a contaminated site. RESULTS: The pre-concentration method enabled determination of carbon isotope ratios (δ(13)C values) of HCH isomers with no significant isotopic fractionation. The TG-HCH mixtures had significantly different δ(13)C values. Moreover, for any given TG-HCH, all isomers had δ(13)C values within 1.1‰ of each other - a distinctly uniform fingerprint. At the HCH-contaminated field site, compared with source wells, downgradient wells showed significant (up to 5.1‰) enrichment in (13)C and the δ(13)C values of the HCH isomers were significantly different from each other. CONCLUSIONS: A method was successfully developed for the CSIA of HCH isomers that showed potential for HCH source differentiation and identification of HCH in situ biodegradation. At the HCH-contaminated site, the observed preferential isotopic enrichment of certain isomers relative to others for a given source allows differentiation between biodegraded and non-biodegraded HCH.

Diffusion sampler for compound specific carbon isotope analysis of dissolved hydrocarbon contaminants.

Compound Specific Isotope Analysis (CSIA) is widely utilized to study the fate of organic contaminants in groundwater. To date, however, no method is available to obtain CSIA samples at a fine (cm) spatial scale across the sediment-surface water interface (SWI), a key boundary for discharge of contaminated groundwater to surface water. Dissolved contaminants in such discharged zones undergo rapid temporal and spatial changes due to heterogeneity in redox conditions and microbial populations. The compatibility of a passive sediment pore water sampler ("peeper") to collect 40 mL samples for CSIA of benzene, toluene, monochlorobenzene, and 1,2-dichlorobenzene at field-relevant concentrations (0.1-5 mg L(-1)) was evaluated in laboratory experiments. Results demonstrate that physical diffusion across the polysulfone membrane does not alter the carbon isotope values (±0.5‰). Measured δ(13)C values also remain invariant despite significant adsorption of the compounds on the peeper material, an effect which increased with higher numbers of chlorine atoms and sorption coefficient (Koc) values. In addition, isotope equilibrium between the peeper chamber and the sediment pore water occurred in less than a day, indicating the peeper method can be used to provide samples for CSIA analysis at fine spatial and temporal sampling resolutions in contaminated sediments.

Distinct carbon isotope fractionation during anaerobic degradation of dichlorobenzene isomers.

Chlorinated benzenes are ubiquitous organic contaminants found in groundwater and soils. Compound specific isotope analysis (CSIA) has been increasingly used to assess natural attenuation of chlorinated contaminants, in which anaerobic reductive dechlorination plays an essential role. In this work, carbon isotope fractionation of the three dichlorobenzene (DCB) isomers was investigated during anaerobic reductive dehalogenation in methanogenic laboratory microcosms. Large isotope fractionation of 1,3-DCB and 1,4-DCB was observed while only a small isotope effect occurred for 1,2-DCB. Bulk enrichment factors (εbulk) were determined from a Rayleigh model: -0.8 ± 0.1 ‰ for 1,2-DCB, -5.4 ± 0.4 ‰ for 1,3-DCB, and -6.3 ± 0.2 ‰ for 1,4-DCB. εbulk values were converted to apparent kinetic isotope effects for carbon (AKIE) in order to characterize the carbon isotope effect at the reactive positions for the DCB isomers. AKIE values are 1.005 ± 0.001, 1.034 ± 0.003, and 1.039 ± 0.001 for 1,2-DCB, 1,3-DCB, and 1,4-DCB, respectively. The large difference in AKIE values between 1,2-DCB and 1,3-DCB (or 1,4-DCB) suggests distinct reaction pathways may be involved for different DCB isomers during microbial reductive dechlorination by the methanogenic cultures.

Ecological engineering practices for the reduction of excess nitrogen in human-influenced landscapes: a guide for watershed managers.

Excess nitrogen (N) in freshwater systems, estuaries, and coastal areas has well-documented deleterious effects on ecosystems. Ecological engineering practices (EEPs) may be effective at decreasing nonpoint source N leaching to surface and groundwater. However, few studies have synthesized current knowledge about the functioning principles, performance, and cost of common EEPs used to mitigate N pollution at the watershed scale. Our review describes seven EEPs known to decrease N to help watershed managers select the most effective techniques from among the following approaches: advanced-treatment septic systems, low-impact development (LID) structures, permeable reactive barriers, treatment wetlands, riparian buffers, artificial lakes and reservoirs, and stream restoration. Our results show a broad range of N-removal effectiveness but suggest that all techniques could be optimized for N removal by promoting and sustaining conditions conducive to biological transformations (e.g., denitrification). Generally, N-removal efficiency is particularly affected by hydraulic residence time, organic carbon availability, and establishment of anaerobic conditions. There remains a critical need for systematic empirical studies documenting N-removal efficiency among EEPs and potential environmental and economic tradeoffs associated with the widespread use of these techniques. Under current trajectories of N inputs, land use, and climate change, ecological engineering alone may be insufficient to manage N in many watersheds, suggesting that N-pollution source prevention remains a critical need. Improved understanding of N-removal effectiveness and modeling efforts will be critical in building decision support tools to help guide the selection and application of best EEPs for N management.

Modeling multi-year phosphorus dynamics in a bioretention cell: Phosphorus partitioning, accumulation, and export.

Phosphorus (P) export from urban areas via stormwater runoff contributes to eutrophication of downstream aquatic ecosystems. Bioretention cells are a Low Impact Development (LID) technology promoted as a green solution to attenuate urban peak flow discharge, as well as the export of excess nutrients and other contaminants. Despite their rapidly growing implementation worldwide, a predictive understanding of the efficiency of bioretention cells in reducing urban P loadings remains limited. Here, we present a reaction-transport model to simulate the fate and transport of P in a bioretention cell facility in the greater Toronto metropolitan area. The model incorporates a representation of the biogeochemical reaction network that controls P cycling within the cell. We used the model as a diagnostic tool to determine the relative importance of processes immobilizing P in the bioretention cell. The model predictions were compared to multi-year observational data on 1) the outflow loads of total P (TP) and soluble reactive P (SRP) during the 2012-2017 period, 2) TP depth profiles collected at 4 time points during the 2012-2019 period, and 3) sequential chemical P extractions performed on core samples from the filter media layer obtained in 2019. Results indicate that exfiltration to underlying native soil was principally responsible for decreasing the surface water discharge from the bioretention cell (63 % runoff reduction). From 2012 to 2017, the cumulative outflow export loads of TP and SRP only accounted for 1 % and 2 % of the corresponding inflow loads, respectively, hence demonstrating the extremely high P reduction efficiency of this bioretention cell. Accumulation in the filter media layer was the predominant mechanism responsible for the reduction in P outflow loading (57 % retention of TP inflow load) followed by plant uptake (21 % TP retention). Of the P retained within the filter media layer, 48 % occurred in stable, 41 % in potentially mobilizable, and 11 % in easily mobilizable forms. There were no signs that the P retention capacity of the bioretention cell was approaching saturation after 7 years of operation. The reactive transport modeling approach developed here can in principle be transferred and adapted to fit other bioretention cell designs and hydrological regimes to estimate P surface loading reductions at a range of temporal scales, from a single precipitation event to long-term (i.e., multi-year) operation.

Development of a constructed wetland water treatment system for selenium removal: use of mesocosms to evaluate design parameters.

The Salton Sea in California is an important habitat for fish and waterfowl. Its ecosystem is threatened due to diminishing water supplies and increasing salinity. An alternative source of water to support species conservation habitat may be obtained from local rivers (e.g., Alamo or New Rivers), provided that a wetland treatment system can be developed to remove selenium (Se), fertilizer nutrients, and other contaminants. Here, we used mesocosms to evaluate a number of potential design options (e.g., plant species selection, sediment composition and arrangement, forced aeration, organic amendments, etc.) to improve the efficiency of Se removal using treatment wetlands. Our results show that, of five different substrate arrangements tested for Se removal, the most efficient was obtained for cattails growing in a substrate of cattail litter overlying sand and peat moss sediment (water column Se was reduced from 15 µg Se/L to <0.1 µg Se/L in 72 h). The addition of organic amendments in the form of alfalfa hay or alfalfa meal was also helpful in lowering Se levels. These results suggest that it may be possible to design constructed wetland water treatment systems capable of reducing Se concentrations in river water to values below 1 µg Se/L.

Implications of polar organic chemical integrative sampler for high membrane sorption and suitability of polyethersulfone as a single-phase sampler.

Polar organic chemical integrative sampler (POCIS) contains sorbent, which is typically enclosed between two polyethersulfones (PES) membranes. A significant PES uptake is reported for many contaminants, yet, aqueous concentration is mainly correlated with the sorbent uptake using first-order kinetics. Under high PES sorption, the first-order kinetics often provide erroneous sampling rate for the sorbent phase due to increased membrane resistance. This work evaluated the uptake of four high PES sorbing chemicals, i.e., three Cl- and CH3-substituted nitrobenzenes and one chlorinated aniline using POCIS and the potential of a single-phase PES sampler using laboratory experiments. POCIS calibration results demonstrated that both sorbent and membrane had similar affinity for the target compounds. A rapid PES sorption occurred in the earlier days (<7 days) followed by a gradual increase in the PES phase concentration (equilibrium not achieved after 60 days). Especially, the membrane was the primary sink for 3,4-dichloroaniline and 3,4-dichloronitrobenzene for up to 14 and 31 days, respectively. On the other hand, the single-phase PES sampler showed similar mass uptake as POCIS and reached equilibrium within 19 days under static condition, indicating its potential suitability in the equilibrium regime. PES-water partition coefficient of the target compounds was between 1.2 and 6.5 L/g. Finally, we present a poly-parameter linear-free energy relationship (pp-LFER) using published data to predict the PES-water partition coefficients. The pp-LFER models showed moderate predictability as indicated by R2adj values between 0.7 and 0.9 for both internal and external data set consisting of a wide range of hydrophobic and hydrophilic compounds (-0.1 ≤ logKOW ≤ 7.4). The proposed pp-LFER model can be used to screen high PES-sorbing chemicals to increase the reliability and accuracy of aqueous concentration prediction from POCIS sampling and to select the most appropriate sampling approach for new compounds.

Evaluating perfluorooctanoic acid (PFOA) and perfluorooctanesulfonic acid (PFOS) removal across granular activated carbon (GAC) filter-adsorbers in drinking water treatment plants.

Granular activated carbon (GAC) was harvested from six filter-adsorbers that are used for taste and odour control in three drinking water treatment plants in Ontario, Canada, and evaluated for the removal of perfluorooctanic acid (PFOA) and perfluorooctanesulfonic acid (PFOS) using minicolumn tests under different operational conditions. Parallel column tests were conducted using unsterilized GAC and sterilized GAC to distinguish adsorption from potential biodegradation of PFOA and PFOS across the GAC. It was observed that the GAC could achieve approximately 20% to 55% of PFOA and PFOS removal even after a long period of GAC operation (e.g., 6 years). There was no evidence of PFOA and PFOS biodegradation, so the removal in GAC can be attributed solely to adsorption under the conditions tested. However, in one location, there was evidence suggesting both removal and formation of PFOS and PFOA across the GAC, with the formation presumably due to the biotransformation of pre-existing precursors in the source water. Additionally, GAC service time and empty bed contact time (EBCT) were identified to be important factors that could affect the removal of PFOA and PFOS. Based on this information, an empirical model was proposed to predict PFOA and PFOS removal in GAC filter-adsorbers as a function of GAC service time and EBCT. This study provides useful information for utilities that have installed GAC for taste and odour control but may consider per- and polyfluoroalkyl substances (PFAS) removal as an additional voluntary objective or due to more stringent guidelines.

Understanding adsorption and biodegradation in granular activated carbon for drinking water treatment: A critical review.

Drinking water treatment plants use granular activated carbon (GAC) to adsorb and remove trace organics, but the GAC has a limited lifetime in terms of adsorptive capacity and needs to be replaced before it is exhausted. Biological degradation of target contaminants can also occur in GAC filters, which might allow the GAC to remain in service longer than expected. However, GAC biofiltration remains poorly understood and unpredictable. To increase the understanding of adsorption and biodegradation in GAC, previous studies have conducted parallel column tests that use one column of GAC (potentially biologically active) to assess overall removal via both adsorption and biodegradation, and one column with either sterilized GAC or biological non-adsorbing media to assess adsorption or biodegradation alone. Mathematical models have also been established to give insight into the adsorption and biodegradation processes in GAC. In this review, the experimental and modeling approaches and results used to distinguish between the role of adsorption and biodegradation were summarized and critically discussed. We identified several limitations: (1) using biological non-adsorbing media in column tests might lead to non-representative extents of biodegradation; (2) sterilization methods may not effectively inhibit biological activity and may affect adsorption; (3) using virgin GAC coated with biofilm could overestimate adsorption; (4) potential biofilm detachment during column experiments could lead to biased results; (5) the parallel column test approach itself is not universally applicable; (6) competitive adsorption was neglected by previous models; (7) model formulations were based on virgin GAC only. To overcome these limitations, we proposed four new approaches: the use of gamma irradiation for sterilization, a novel minicolumn test, compound-specific isotope analysis to decipher the role of adsorption and biodegradation in situ, and a new model to simulate trace organic adsorption and biodegradation in a GAC filter .

Evaluating the relative adsorption and biodegradation of 2-methylisoborneol and geosmin across granular activated carbon filter-adsorbers.

This study investigated the relative contributions of adsorption vs. biodegradation towards 2-methylisoborneol (MIB) and geosmin removal in the granular activated carbon (GAC) harvested from six filter-adsorbers in three drinking water treatment plants in the Great Lakes region. Column tests using azide-treated (sterilized) and untreated GAC in parallel were used to isolate the two effects. It was identified that substantial MIB and geosmin biodegradation in the GAC was occurring in one location, and that GAC in some cases had significant adsorption capacity after as much as 9 years of operation. Four alternative biological parameters (adenosine triphosphate, esterase activity, phosphatase activity, and 14C-glucose respiration rate) were measured to quantify the biological activity of the GAC, and 14C-glucose respiration rate was identified to be a potential indicator for GAC biodegradative capacity in terms of MIB, geosmin, and dissolved organic carbon. Several potential MIB and geosmin biodegradation products were also identified using non-targeted screening analysis. By using the new tools identified in this study, we can begin to better understand where adsorption vs. biodegradation may predominate under real-world conditions (e.g., different temperatures, influent concentrations, and empty bed contact time), leading ultimately to more cost-effective use of GAC.

Triclosan uptake and transformation by the green algae Euglena gracilis strain Z.

Triclosan is an antimicrobial chemical present in consumer products that is frequently detected in aquatic environments. In this research, we investigated the role of a common freshwater microalgae species, Euglena gracilis for triclosan uptake and transformation in open-water treatment wetlands. Lab-scale wetland bioreactors were created under various conditions of light (i.e., continuous (white) light, red light, and in the dark), media (i.e., wetland, autoclaved wetland, Milli-Q, and growth media water), and presence or absence of algae. Triclosan and its potential transformation products were identified in the water and algae phases. Triclosan transformation occurred most rapidly with reactors that received continuous (white) light, with pseudo first-order rate constants, k, ranging from 0.035 to 0.292 day-1. This indicates that phototransformation played a major role in triclosan transformation during the day, despite light screening by algae. Algae contributed to the uptake and transformation of triclosan in all reactors, and algae and bacteria both contributed to triclosan biotransformation under dark conditions, representative of nighttime conditions. Some transformation products were formed and further transformed, e.g., triclosan-O-sulfate, methoxy and diglucosyl conjugate of hydroxylated triclosan, and dimethoxy and glucosyl conjugate of 2,4-dichlorophenol, suggesting their minimal accumulation over the 25 days of the experiments. This study shows that the combined action of light, microbes, and algae allows the safe transfer and transformation of triclosan in open-water treatment wetlands.