Influence of Divalent Cation Inhibition and Dissolved Organic Matter Enhancement on Phenol Oxidation Kinetics by Manganese Oxides.

Manganese oxides can oxidize organic compounds, such as phenols, and may potentially be used in passive water treatment applications. However, the impact of common water constituents, including cations and dissolved organic matter (DOM), on this reaction is poorly understood. For example, the presence of DOM can increase or decrease phenol oxidation rates with manganese oxides. Furthermore, the interactions of DOM and cations and their impact on the phenol oxidation rates have not been examined. Therefore, we investigated the oxidation kinetics of six phenolic contaminants with acid birnessite in ten whole water samples. The oxidation rate constants of 4-chlorophenol, 4-tert-octylphenol, 4-bromophenol, and phenol consistently decreased in all waters relative to buffered ultrapure water, whereas the oxidation rate of bisphenol A and triclosan increased by up to 260% in some waters. Linear regression analyses and targeted experiments demonstrated that the inhibition of phenol oxidation is largely determined by cations. Furthermore, quencher experiments indicated that radical-mediated interactions from oxidized DOM contributed to enhanced oxidation of bisphenol A. The variable changes between compounds and water samples demonstrate the challenge of accurately predicting contaminant transformation rates in environmentally relevant systems based on experiments conducted in the absence of natural water constituents.

Laboratory measurements underestimate persistence of the aquatic herbicide fluridone in lakes.

Fluridone is an aquatic herbicide commonly used to treat invasive freshwater plant species such as Eurasian watermilfoil, hydrilla, and curly-leaf pondweed. However, required exposures times are very long and often exceed 100 days. Thus, understanding the mechanisms that determine the fate of fluridone in lakes is critical for supporting effective herbicide treatments and minimizing impacts to non-target species. We use a combination of laboratory and field studies to quantify fluridone photodegradation, as well as sorption and microbial degradation in water and sediment microcosms. Laboratory irradiation studies demonstrate that fluridone is susceptible to direct photodegradation with negligible indirect photodegradation, with predicted half-lives in sunlight ranging from 2.3 days (1 cm path length) to 118 days (integrated over 1 meter). Biodegradation is attributable to microbes in sediment with an observed half-life of 57 days. Lastly, fluridone sorbs to sediments (Koc = 340 ± 28 L kg-1); sorption accounts for 16% of fluridone loss in the microcosm experiments. While the laboratory results indicate that all three loss pathways can influence fluridone fate, these controlled studies oversimplify herbicide behavior due to their inability to replicate field conditions. Fluridone concentration measurements in a lake following commercial application demonstrate a half-life of >150 days, indicating that the herbicide is very persistent in water. This study illustrates why caution should be used when relying on laboratory studies to predict the fate of pesticides and other polar organic compounds in the environment.

Limitations of conventional approaches to identify photochemically produced reactive intermediates involved in contaminant indirect photodegradation.

Dissolved organic matter (DOM) mediated indirect photodegradation can play an important role in the degradation of aquatic contaminants. Predicting the rate of this process requires knowledge of the photochemically produced reactive intermediates (PPRI) that react with the compound of interest, as well as the ability of individual DOM samples to produce PPRI. Key PPRI are typically identified using quencher studies, yet this approach often leads to results that are difficult to interpret. In this work, we analyze the indirect photodegradation of atorvastatin, carbamazepine, sulfadiazine, and benzotriazole using a diverse set of 48 waters from natural and engineered aquatic systems. We use this large data set to evaluate relationships between PPRI formation and indirect photodegradation rate constants, which are directly compared to results using standard quenching experiments. These data demonstrate that triplet state DOM (3DOM) and singlet oxygen (1O2) are critical PPRI for atorvastatin, carbamazepine, and sulfadiazine, while hydroxyl radical (˙OH) contributes to the indirect photodegradation of benzotriazole. We caution against relying on quenching studies because quenching of 3DOM limits the formation of 1O2 and all studied quenchers react with ˙OH. Furthermore, we show that DOM composition directly influences indirect photodegradation and that low molecular weight, microbial-like DOM is positively correlated with the indirect photodegradation rates of carbamazepine, sulfadiazine, and benzotriazole.

Quantifying the Role of Simultaneous Transformation Pathways in the Fate of the Novel Aquatic Herbicide Florpyrauxifen-Benzyl.

Predicting the fate of organic compounds in the environment is challenging due to the inability of laboratory studies to replicate field conditions. We used the intentionally applied aquatic herbicide florpyrauxifen-benzyl (FPB) as a model compound to investigate the contribution of multiple transformation pathways to organic compound fate in lakes. FPB persisted in five Wisconsin lakes for 5-7 days with an in-lake half-life of <2 days. FPB formed four transformation products, with the bioactive product florpyrauxifen persisting up to 30 days post-treatment. Parallel laboratory experiments showed that FPB degrades to florpyrauxifen via base-promoted hydrolysis. Hydroxy-FPB and hydroxy-florpyrauxifen were identified as biodegradation products, while dechloro-FPB was identified as a photoproduct. Material balance calculations using both laboratory rates and field product concentrations demonstrated that hydrolysis (∼47% of loss), biodegradation (∼20%), sorption (∼13%), and photodegradation (∼4%) occurred on similar timescales. Furthermore, the combined results demonstrated that abiotic and plant-catalyzed hydrolysis of FPB to florpyrauxifen, followed by biodegradation of florpyrauxifen to hydroxy-florpyrauxifen, was the dominant transformation pathway in lakes. This study demonstrates how combined field and laboratory studies can be used to elucidate the role of simultaneous and interacting pathways in the fate of organic compounds in aquatic environments.

Dissolved Organic Matter Composition Determines Its Susceptibility to Complete and Partial Photooxidation within Lakes.

Dissolved organic matter (DOM) plays an important role in carbon cycling within inland surface waters. Under sunlight irradiation, DOM undergoes complete photooxidation to produce carbon dioxide (CO2) and partial photooxidation that alters the molecular composition of DOM. However, a mechanistic understanding of the relationship between DOM composition and its susceptibility to partial and complete photooxidation in surface waters is currently lacking. This work combines light exposure experiments with high-resolution mass spectrometry to investigate DOM photooxidation using two DOM isolates and DOM from 16 lakes that vary in trophic status and size. High ratios of oxygen consumption to dissolved inorganic carbon (DIC) production demonstrate that all samples undergo extensive partial photooxidation. At the molecular level, more oxidized, aromatic DOM formulas are associated with oxygen consumption and DIC production. Bulk level measurements indicate that DOM becomes less aromatic and lower in apparent molecular weight following partial photooxidation, and there is molecular level evidence of oxygen addition and loss of CO2 in all samples. However, formulas most susceptible to photooxidation vary depending on the initial DOM composition. Collectively, this work provides insights into the relationship between DOM composition and photooxidation, which has important implications for carbon cycling in diverse surface waters.

Formation of Targeted and Novel Disinfection Byproducts during Chlorine Photolysis in the Presence of Bromide.

Chlorine photolysis is an advanced oxidation process that relies on the combination of direct chlorination by free available chlorine, direct photolysis, and reactive oxidants to transform contaminants. In waters that contain bromide, free available bromine and reactive bromine species can also form. However, little is known about the underlying mechanisms or formation potential of disinfection byproducts (DBPs) under these conditions. We investigated reactive oxidant generation and DBP formation under dark conditions, chlorine photolysis, and radical-quenched chorine photolysis with variable chlorine (0-10 mg-Cl2/L) and bromide (0-2,000 µg/L) concentrations, as well as with free available bromine. Probe loss rates and ozone concentrations increase with chlorine concentration and are minimally impacted by bromide. Radical-mediated processes partially contribute to the formation targeted DBPs (i.e., trihalomethanes, haloacetic acids, haloacetonitriles, chlorate, and bromate), which increase with increasing chlorine concentration. Chlorinated novel DBPs detected by high-resolution mass spectrometry are attributable to a combination of dark chlorination, direct halogenation by reactive chlorine species, and transformation of precursors, whereas novel brominated DBPs are primarily attributable to dark bromination of electron-rich formulas. The formation of targeted and novel DBPs during chlorine photolysis in waters with elevated bromide may limit treatment applications.

Dissolved Organic Matter Photoreactivity Is Determined by Its Optical Properties, Redox Activity, and Molecular Composition.

Predicting the formation of photochemically produced reactive intermediates (PPRI) during the irradiation of dissolved organic matter (DOM) has remained challenging given the complex nature of this material and differences in PPRI formation mechanisms. We investigate the role of DOM composition in photoreactivity using 48 samples that span the range of DOM in freshwater systems and wastewater. We relate quantum yields for excited triplet-state organic matter (fTMP), singlet oxygen (Φ1O2), and hydroxylating species (Φ•OH) to DOM composition determined using spectroscopy, Fourier-transform ion cyclotron resonance mass spectrometry, and electron-donating capacity (EDC). fTMP and Φ1O2 follow similar trends and are correlated with bulk properties derived from UV-vis spectra and EDC. In contrast, no individual bulk property can be used to predict Φ•OH. At the molecular level, the subset of DOM that is positively correlated to both Φ•OH and EDC is distinct from DOM formulas related to Φ1O2, demonstrating that •OH and 1O2 are formed from different DOM fractions. Multiple linear regressions are used to relate quantum yields of each PPRI to DOM composition parameters derived from multiple techniques, demonstrating that complementary methods are ideal for characterizing DOM because each technique only samples a subset of DOM.

Impacts of Environmental and Engineered Processes on the PFAS Fingerprint of Fluorotelomer-Based AFFF.

Forensic analysis can potentially be used to determine per- and polyfluoroalkyl substance (PFAS) sources at contaminated sites. However, fluorotelomer aqueous film-forming foam (AFFF) sources are difficult to identify because the polyfluorinated active ingredients do not have authentic standards and because the parent compounds can undergo transformation and differential transport, resulting in alteration of the PFAS distribution or fingerprint. In this study, we investigate changes in the PFAS fingerprint of fluorotelomer-derived AFFF due to environmental and engineered processes, including groundwater transport, surface water flow, and land application of contaminated biosolids. Fingerprint analysis supplemented by quantification of precursors and identification of suspected active ingredients shows a clear correlation between a fluorotelomer AFFF manufacturer and surface water of nearby Lake Michigan, demonstrating contamination (>100 ng/L PFOA) of the lake due to migration of an AFFF-impacted groundwater plume. In contrast, extensive processing during wastewater treatment and environmental transport results in large changes to the AFFF fingerprint near agricultural fields where contaminated biosolids were spread. At biosolids-impacted sites, the presence of active ingredients confirms contamination by fluorotelomer AFFF. While sediments can retain longer-chain PFAS, this study demonstrates that aqueous samples are most relevant for PFAS fingerprinting in complex sites, particularly where shorter-chain compounds have been used.

Impact of ozone-biologically active filtration on the breakthrough of Perfluoroalkyl acids during granular activated carbon treatment of municipal wastewater effluent.

The presence of perfluoroalkyl acids (PFAAs) in municipal wastewater has highlighted the need to develop PFAA treatment approaches for wastewater effluent and potable reuse applications. Ozone (O3) and biologically active filtration (BAF) were investigated as standalone and combined pretreatment processes to improve the performance of granular activated carbon (GAC) for PFAA removal from wastewater effluent. As individual processes, ozonation at all three investigated doses (0.35, 0.75, 1.0 mg O3/mg DOC) and BAF at both tested empty bed contact times (EBCT; 15 and 20 min) led to significant improvement in PFAA removal by subsequent GAC treatment. With respect to standalone ozonation, the specific O3 dose of 0.75 mg O3/mg DOC was proven to be the optimum operating condition as further increase of the specific ozone dose to 1.0 mg O3/mg DOC did not provide considerable additional improvement. Extending the EBCT during standalone BAF from 15 to 20 minutes significantly improved the efficacy of GAC for the removal of tested PFAAs. Pretreatment with O3-BAF (0.75 mg O3/mg DOC; 20 min EBCT) in tandem outperformed both standalone ozonation and BAF for the removal of PFAA by GAC. Characterization of effluent organic matter (EfOM) by size exclusion chromatography (SEC) and Fourier transform-ion cyclotron resonance mass spectrometry (FT-ICR-MS) before and after pretreatments suggest that among multiple co-occurring phenomena, the shift towards smaller and more polar EfOM may have predominantly alleviated pore constriction/blockage without having adverse impact on direct site competition. This observation is supported by SEC and FT-ICR-MS results indicating reduced EfOM molecular size through O3 and BAF pretreatment as well as transition to more hydrophilic byproducts.

Synthesizing Laboratory and Field Experiments to Quantify Dominant Transformation Mechanisms of 2,4-Dichlorophenoxyacetic Acid (2,4-D) in Aquatic Environments.

Laboratory studies used to assess the environmental fate of organic chemicals such as pesticides fail to replicate environmental conditions, resulting in large errors in predicted transformation rates. We combine laboratory and field data to identify the dominant loss processes of the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D) in lakes for the first time. Microbial and photochemical degradation are individually assessed using laboratory-based microcosms and irradiation studies, respectively. Field campaigns are conducted in six lakes to quantify 2,4-D loss following large-scale herbicide treatments. Irradiation studies show that 2,4-D undergoes direct photodegradation, but modeling efforts demonstrated that this process is negligible under environmental conditions. Microcosms constructed using field inocula show that sediment microbial communities are responsible for degradation of 2,4-D in lakes. Attempts to quantify transformation products are unsuccessful in both laboratory and field studies, suggesting that their persistence is not a major concern. The synthesis of laboratory and field experiments is used to demonstrate best practices in designing laboratory persistence studies and in using those results to mechanistically predict contaminant fate in complex aquatic environments.

Selective Reactivity and Oxidation of Dissolved Organic Matter by Manganese Oxides.

Dissolved organic matter (DOM) varies widely across natural and engineered systems, but little is known about the influence of DOM composition on its reactivity with manganese oxides. Here, we investigate bulk and molecular transformations of 30 diverse DOM samples after reaction with acid birnessite (MnO2), a strong oxidant that may react with DOM in Mn-rich environments or engineered treatment systems. The reaction of DOM with acid birnessite reduces Mn and forms DOM that is generally more aliphatic and lower in apparent molecular weight. However, the extent of reaction depends on the water type (e.g., wastewater, rivers) and highly aromatic DOM undergoes greater changes. Despite the variability in reactivity due to the DOM composition, aqueous products attributable to the oxidation of phenolic precursors are identified in waters analyzed by high-resolution mass spectrometry. The number of matched product formulas correlates significantly with indicators of DOM aromaticity, such as double-bond equivalents (p = 2.43 × 10-4). At the molecular level, highly aromatic, lignin-like carbon reacts selectively with acid birnessite in all samples despite the variability in initial DOM composition, resulting in the formation of a wide range of aqueous products. These findings demonstrate that DOM oxidation occurs in diverse waters but also suggest that reactivity with acid birnessite and the composition of the resulting aqueous DOM pool are composition-dependent and linked to the DOM source and initial aromaticity.

Chlorinated Byproduct Formation during the Electrochemical Advanced Oxidation Process at Magnéli Phase Ti4O7 Electrodes.

This research investigated chlorinated byproduct formation at Ti4O7 anodes. Resorcinol was used as a model organic compound representative of reactive phenolic groups in natural organic matter and industrial phenolic contaminants and was oxidized in the presence of NaCl (0-5 mM). Resorcinol mineralization was >68% in the presence and absence of NaCl at 3.1 V/SHE (residence time = 13 s). Results indicated that ∼4.3% of the initial chloride was converted to inorganic byproducts (free Cl2, ClO2-, ClO3-) in the absence of resorcinol, and this value decreased to <0.8% in the presence of resorcinol. Perchlorate formation rates from chlorate oxidation were 115-371 mol m-2 h-1, approximately two orders of magnitude lower than reported values for boron-doped diamond anodes. Liquid chromatography-mass spectroscopy detected two chlorinated organic products. Multichlorinated alcohol compounds (C3H2Cl4O and C3H4Cl4O) at 2.5 V/SHE and a monochlorinated phenolic compound (C8H7O4Cl) at 3.1 V/SHE were proposed as possible structures. Density functional theory calculations estimated that the proposed alcohol products were resistant to direct oxidation at 2.5 V/SHE, and the C8H7O4Cl compound was likely a transient intermediate. Chlorinated byproducts should be carefully monitored during electrochemical advanced oxidation processes, and multibarrier treatment approaches are likely necessary to prevent halogenated byproducts in the treated water.

Molecular-Level Transformation of Dissolved Organic Matter during Oxidation by Ozone and Hydroxyl Radical.

Ozonation of drinking and wastewater relies on ozone (O3) and hydroxyl radical (•OH) as oxidants. Both oxidants react with dissolved organic matter (DOM) and alter its composition, but the selectivity of the two oxidants and mechanisms of reactivity with DOM moieties are largely unknown. The reactions of O3 and •OH with two DOM isolates were studied by varying specific ozone doses (0.1-1.3 mg-O3/mg-C) at pH 7. Additionally, conditions that favor O3 (i.e., addition of an •OH scavenger) or •OH (i.e., pH 11) were investigated. Ozonation decreases aromaticity, apparent molecular weight, and electron donating capacity (EDC) of DOM with large changes observed when O3 is the main oxidant (e.g., EDC decreases 63-77% for 1.3 mg-O3/mg-C). Both O3 and •OH react with highly aromatic, reduced formulas detected using high-resolution mass spectrometry (O:C = 0.48 ± 0.12; H:C = 1.06 ± 0.23), while •OH also oxidizes more saturated formulas (H:C = 1.64 ± 0.26). Established reactions between model compounds and O3 (e.g., addition of one to two oxygen atoms) or •OH (e.g., addition of one oxygen atom and decarboxylation) are observed and produce highly oxidized DOM (O:C > 1.0). This study provides molecular-level evidence for the selectivity of O3 as an oxidant within DOM.

Role of Reactive Halogen Species in Disinfection Byproduct Formation during Chlorine Photolysis.

The multiple reactive oxidants produced during chlorine photolysis effectively degrade organic contaminants during water treatment, but their role in disinfection byproduct (DBP) formation is unclear. The impact of chlorine photolysis on dissolved organic matter (DOM) composition and DBP formation is investigated using lake water collected after coagulation, flocculation, and filtration at pH 6.5 and pH 8.5 with irradiation at three wavelengths (254, 311, and 365 nm). The steady-state concentrations of hydroxyl radical and chlorine radical decrease by 38-100% in drinking water compared to ultrapure water, which is primarily attributed to radical scavenging by natural water constituents. Chlorine photolysis transforms DOM through multiple mechanisms to produce DOM that is more aliphatic in nature and contains novel high molecular weight chlorinated DBPs that are detected via high-resolution mass spectrometry. Quenching experiments demonstrate that reactive chlorine species are partially responsible for the formation of halogenated DOM, haloacetic acids, and haloacetonitriles, whereas trihalomethane formation decreases during chlorine photolysis. Furthermore, DOM transformation primarily due to direct photolysis alters DOM such that it is more reactive with chlorine, which also contributes to enhanced formation of novel DBPs during chlorine photolysis.

Potential changes to the biology and challenges to the management of invasive sea lamprey Petromyzon marinus in the Laurentian Great Lakes due to climate change.

Control programs are implemented to mitigate the damage caused by invasive species worldwide. In the highly invaded Great Lakes, the climate is expected to become warmer with more extreme weather and variable precipitation, resulting in shorter iced-over periods and variable tributary flows as well as changes to pH and river hydrology and hydrogeomorphology. We review how climate change influences physiology, behavior, and demography of a damaging invasive species, sea lamprey (Petromyzon marinus), in the Great Lakes, and the consequences for sea lamprey control efforts. Sea lamprey control relies on surveys to monitor abundance of larval sea lamprey in Great Lakes tributaries. The abundance of parasitic, juvenile sea lampreys in the lakes is calculated by surveying wounding rates on lake trout (Salvelinus namaycush), and trap surveys are used to enumerate adult spawning runs. Chemical control using lampricides (i.e., lamprey pesticides) to target larval sea lamprey and barriers to prevent adult lamprey from reaching spawning grounds are the most important tools used for sea lamprey population control. We describe how climate change could affect larval survival in rivers, growth and maturation in lakes, phenology and the spawning migration as adults return to rivers, and the overall abundance and distribution of sea lamprey in the Great Lakes. Our review suggests that Great Lakes sea lamprey may benefit from climate change with longer growing seasons, more rapid growth, and greater access to spawning habitat, but uncertainties remain about the future availability and suitability of larval habitats. Consideration of the biology of invasive species and adaptation of the timing, intensity, and frequency of control efforts is critical to the management of biological invasions in a changing world, such as sea lamprey in the Great Lakes.

Identifying the mechanisms of cation inhibition of phenol oxidation by acid birnessite.

Many phenolic compounds found as contaminants in natural waters are susceptible to oxidation by manganese oxides. However, there is often variability between oxidation rates reported in pristine matrices and studies using more environmentally relevant conditions. For example, the presence of cations generally results in slower phenolic oxidation rates. However, the underlying mechanism of cation interference is not well understood. In this study, cation co-solutes inhibit the transformation of four target phenols (bisphenol A, estrone, p-cresol, and triclosan) by acid birnessite. Oxidation rates for these compounds by acid birnessite follow the same trend (Na+ > K+ > Mg2+ > Ca2+) when cations are present as co-solutes. We further demonstrate that the same trend applies to these cations when they are absent from solution but pre-exchanged with the mineral. We analyze valence state, surface area, crystallinity, and zeta potential to characterize changes in oxide structure. The findings of this study show that pre-exchanged cations have a large effect on birnessite reactivity even in the absence of cation co-solutes, indicating that the inhibition of phenolic compound oxidation is not due to competition for surface sites, as previously suggested. Instead, the reaction inhibition is attributed to changes in aggregation and the mineral microstructure.

The Role of Dissolved Organic Matter Composition in Determining Photochemical Reactivity at the Molecular Level.

Dissolved organic matter (DOM) composition influences its ability to form photochemically produced reactive intermediates (PPRI). While relationships have been established between bulk DOM properties and triplet DOM (3DOM) and singlet oxygen (1O2) quantum yields, contradictory evidence exists for hydroxyl radical (•OH) and hydroxylating species. Furthermore, little is known about these relationships at the molecular level. We evaluated DOM composition and photochemical reactivity of water samples from a wastewater treatment plant and the St. Louis River in Minnesota and Wisconsin, U.S.A. Bulk characterization using ultraviolet-visible spectroscopy demonstrates that color and apparent size of DOM decrease downstream, while molecular composition analysis using Fourier-transform ion cyclotron resonance mass spectrometry reveals that saturation and chemodiversity is highest near Lake Superior. 3DOM quantum yield coefficients and 1O2 quantum yields increase downstream and correlate strongly with saturated formulas. Similar results are observed for carbon-normalized photodegradation rate constants of atorvastatin, carbamazepine, and venlafaxine, which react primarily with 3DOM and 1O2. In contrast, •OH quantum yields are lowest downstream and correlate with less saturated, more oxygenated DOM, suggesting that 3DOM is not its major precursor. Mixed relationships are observed for DEET, which reacts with multiple PPRI. Molecular-level compositional data reveal insights into the differing formation pathways of individual PPRI, but information about specific contaminants is needed to predict their photochemical fate.

Spatial and temporal variability of perfluoroalkyl substances in the Laurentian Great Lakes.

Per- and polyfluoroalkyl substances (PFAS) are a diverse group of fluorinated organic chemicals that have been used in industrial and consumer applications since the 1950s. PFAS are resistant to chemical and biological degradation and are ubiquitous in the environment, including in water, sediment, and biota in the Laurentian Great Lakes. This critical review evaluates the spatial and temporal variability of commonly studied perfluoroalkyl sulfonates (PFSAs) and perfluoroalkyl carboxylates (PFCAs) in the Great Lakes by synthesizing data collected in water, surface sediment, sediment cores, lake trout (Salvelinus namaycush), and herring gull (Larus argentatus) eggs. The lowest PFAS concentrations in all matrices are detected in Lake Superior, which is located in the most pristine region of the Great Lakes Basin. In contrast, higher concentrations are observed in Lakes Erie and Ontario, which are more impacted by industrial activity and wastewater discharge. The distribution of individual PFAS compounds also varies across the lakes in response to changes in PFAS sources, with higher proportions of PFSAs in the eastern lakes. Sediment and biota are enriched in long chain PFSAs and PFCAs relative to concentrations in the water column, as expected based on predicted partitioning behavior. Sediment cores and bioarchives consistently demonstrate that PFAS concentrations increased in the Great Lakes from the initial time points until the early 2000s. The available data indicate that PFOS and PFOA concentrations decline after this period in the upper Great Lakes, but are stable in Lake Ontario. However, these trends depend on the lake, the individual compound, and the organism considered.

The Impact of pH and Irradiation Wavelength on the Production of Reactive Oxidants during Chlorine Photolysis.

Chlorine photolysis is an advanced oxidation process which relies on photolytic cleavage of free available chlorine (i.e., hypochlorous acid and hypochlorite) to generate hydroxyl radical, along with ozone and a suite of halogen radicals. Little is known about the impact of wavelength on reactive oxidant generation even though chlorine absorbs light within the solar spectrum. This study investigates the formation of reactive oxidants during chlorine photolysis as a function of pH (6-10) and irradiation wavelength (254, 311, and 365 nm) using a combination of reactive oxidant quantification with validated probe compounds and kinetic modeling. Observed chlorine loss rate constants increase with pH during irradiation at high wavelengths due to the higher molar absorptivity of hypochlorite (p Ka = 7.5), while there is no change at 254 nm. Hydroxyl radical and chlorine radical steady-state concentrations are greatest under acidic conditions for all tested wavelengths and are highest using 254 and 311 nm irradiation. Ozone generation is observed under all conditions, with maximum cumulative concentrations at pH 8 for 311 and 365 nm. A comprehensive kinetic model generally predicts the trends in chlorine loss and oxidant concentrations, but a comparison of previously published kinetic models reveals the challenges of modeling this complex system.

Impact of bisphenol A influent concentration and reaction time on MnO2 transformation in a stirred flow reactor.

Bisphenol A (BPA) is an endocrine disrupting compound commonly found in natural waters at concentrations that are considered harmful for aquatic life. Manganese(iii/iv) oxides are strong oxidants capable of oxidizing organic and inorganic contaminants, including BPA. Here we use δ-MnO2 in stirred flow reactors to determine if higher influent BPA concentrations, or introduction rates, lead to increased polymer production. A major BPA oxidation product, 4-hydroxycumyl alcohol (HCA), is formed through radical coupling, and was therefore used as a metric for polymer production in this study. The influent BPA concentration in stirred flow reactors did not affect HCA yield, suggesting that polymeric production is not strongly dependent on influent concentrations. However, changes in influent BPA concentration affected BPA oxidation rates and the rate of δ-MnO2 reduction. Lower aqueous Mn(ii) production was observed in reactors at higher BPA introduction rates, suggesting that single-electron transfer and polymer production are favored under these conditions. However, an examination of Mn(ii) sorption during these reactions indicated that the length of the reaction, rather than BPA introduction rate, caused enhanced aqueous Mn(ii) production in reactors with low introduction rates and longer reaction times due to increased opportunity for disproportionation and comproportionation. This study demonstrates the importance of investigating both the organic and inorganic reactants in the aqueous and solid phases in this complex reaction.