Hydrophobic Organic Chemicals Research Articles

Efficient zero wastewater and salt-free of cotton fiber dyeing via hydrophobic organic chemical/water two-phase dyeing system

For cotton fabric dyeing, a significant quantity of salt and water are typically consumed in the conventional water dyeing bath. In this study, an environmentally friendly alternative was investigated that could eliminate water waste and salt usage, as well as reducing chemical consumption. This method, which employs a hydrophobic organic chemical/water two-phase dyeing system, solely involves fiber swelling, dye dissolution, and the use of alkaline agents. By substituting the water required for heat and mass with an organic chemical, 71.43% dye reduction can be achieved in dye consumption compared to traditional water-based dyeing method. Benefiting from the natural affinity between dyes and cotton fibers, without any interaction with hydrophobic organic chemicals, reactive dye can diffuse into the fiber surface, which can achieve above 98% dye uptake and 90% fixation rate. The K/S value of the dyed cotton fabric is much higher than that of conventional water bath at the same dye concentration, and it is the highest when the water content is 120 %. Moreover, the uniform distribution of dye and the color fastness of the dyed fabric are comparable to traditional water-based dyeing. Due to the influence of intermolecular forces, the aggregation of dye is changed to varying degrees in different hydrophilic and hydrophobic cotton fiber dyeing systems, which further influences the dyeing quality. This study not only improves the utilization of dye but achieves salt-free, no wastewater emission and reduces the dyeing cost, providing an economical and sustainable dyeing method for the industrial dyeing of cotton fabric.

Improving Sediment Toxicity Testing for Very Hydrophobic Chemicals: Part 1-Spiking, Equilibrating, and Exposure Quantification.

Sediment toxicity tests have applications in ecological risk and chemical safety assessments. Despite the many years of experience in testing and the availability of standard protocols, sediment toxicity testing remains challenging with very hydrophobic organic chemicals (VHOCs; i.e., chemicals with a log octanol/water partition coefficient of more than 6). The challenges primarily relate to the chemicals' low aqueous solubilities and slow kinetics, due to which several experimental artifacts may occur. To investigate the potential artifacts, experiments were performed, focusing on spiking and equilibrating (aging) sediments, as well as exposure quantification with passive sampling. The results demonstrated that generally applied, Organisation for Economic Co-operation and Development-recommended spiking (coating) methods may lead to significant chemical losses and the formation of nondissolved, nonbioavailable VHOCs. Direct spiking appeared to be the most optimal, provided that intensive mixing was applied simultaneously. Passive dosing was tested as a novel way of spiking liquid VHOCs, but the approach proved unsuccessful. Intensive postspiking mixing during sediment equilibration for 1 to 2 weeks was shown to be essential for producing a homogeneous system, minimizing the presence of nondissolved chemical (crystals or nonaqueous phase liquids; NAPLs), and creating a stable toxicological response in subsequent toxicity tests. Finally, exposure quantification of VHOCs in sediments through passive sampling was found to be feasible with different polymers, although prolonged equilibration times may be required, and determining sampler/water partition coefficients can be extremely challenging. The results of additional experiments, focusing on toxicity test exposure duration, concentrations above which NAPLs will occur, and ways to distinguish actual toxicity from false-positive results, are presented in Part 2 of thispublication series. Environ Toxicol Chem 2024;00:1-11. © 2024 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC.

Improving Sediment Toxicity Testing for Very Hydrophobic Chemicals: Part 2-Exposure Duration, Upper Limit Test Concentrations, and Distinguishing Actual Toxicity from Physical Effects.

Sediment toxicity testing with very hydrophobic organic chemicals (VHOCs) is challenging because of the chemicals' low aqueous solubilities and slow kinetics. The present study presents the results of experiments investigating whether the standard exposure duration of 28 days with benthic invertebrates is sufficient for VHOCs; above which concentrations in sediment VHOCs are present as "free phase," that is, crystals or non-aqueous-phase liquids (NAPLs); and whether it is possible to discriminate between actual VHOC toxicity and physical effects caused by NAPLs through fouling of the test organisms. The results suggest that the standard sediment toxicity test duration is sufficient for obtaining steady-state VHOC concentrations in Hyalella azteca and Lumbriculus variegatus, provided that spiking and equilibration are performed properly (i.e., no free phase present). Under these conditions, transient (days 3-20) peak-shaped toxicokinetics were observed, with steady-state concentrations reached at approximately 28 days. The concentration above which NAPLs are present, the so-called critical separate phase concentration (CSPC), was determined for several VHOCs by modeling and two experimental methods. Modeling resulted in unrealistic and variable data and therefore should be applied with caution. Experimentally determining CSPCs was successful and yielded values of approximately 1000 (400-2000) mg/kg dry weight, depending on the chemical. Finally, it was demonstrated that distinguishing actual toxicity from physical effects is possible by applying a well-considered test setup, combining toxicity tests with multiple invertebrates (including Lumbriculus, which serves as a negative control for fouling); a broad test concentration range, preferably up to at least 30 000 mg/kg; and passive sampling to localize the CSPC. Applying this setup, false-positive effects due to fouling, as well as false-negative results due to testing at too low concentrations (trying to stay below the CSPC), can be avoided. Environ Toxicol Chem 2024;00:1-12. © 2023 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC.

Combining Passive Sampling and Dosing to Unravel the Contribution of Hydrophobic Organic Contaminants to Sediment Ecotoxicity.

Contaminated sediments are ubiquitous repositories of pollutants and cause substantial environmental risks. Results of sediment bioassays remain difficult to interpret, however, as observed effects may be caused by a variety of (un)known stressors. This study aimed therefore to isolate the effects of hydrophobic organic contaminants from other (non)chemical stressors present in contaminated sediments, by employing a newly developed passive sampling-passive dosing (PSPD) test. The results showed that equilibrium partitioning between pesticides or polyaromatic hydrocarbons (PAHs) in contaminated sediments and a silicone rubber (SR) passive sampler was achieved after 1-3 days. Chlorpyrifos concentrations in pore water of spiked sediment matched very well with concentrations released from the SR into an aqueous test medium, showing that SR can serve as a passive dosing device. Subjecting the 96 h PSPD laboratory bioassay with nonbiting midge (Chironomus riparius) larvae to field-collected sediments showed that at two locations, concentrations of the hydrophobic organic contaminant mixtures were high enough to affect the test organisms. In conclusion, the developed PSPD test was able to isolate the effects of hydrophobic organic contaminants and provides a promising simplified building block for a suite of PSPD tests that after further validation could be used to unravel the contribution of hydrophobic organic chemicals to sediment ecotoxicity.

How Digestive Processes Can Affect the Bioavailability of PCBs Associated with Microplastics: A Modeling Study Supported by Empirical Data.

The transfer kinetics of plastic-associated chemicals during intestinal digestive processes is unknown. Here, we assessed whether digestive processes affect chemical exchange kinetics on microplastics, using an in vitro gut fluid digestive model mimicking the human upper intestinal tract. Chemical exchange kinetics of microplastics were measured for 10 polychlorinated biphenyls (PCBs) as proxies for the broad class of hydrophobic organic chemicals. Following earlier studies, olive oil was used as a proxy for digestible food, under high and low digestive enzyme activities. The micelle-water and oil-water partition coefficients of the 10 PCBs were also determined to evaluate the relative contribution of each gut component to sorb PCBs. A new biphasic and reversible chemical exchange model, which included the digestion process, fitted well to the empirical data. We demonstrate that the digestive processes that break down contaminated food can lead to a substantial increase in chemical concentration in microplastics by a factor of 10-20, thereby reducing the overall chemical bioavailability in the gastrointestinal tract when compared to a scenario without microplastics. Higher enzyme activities result in more chemicals being released by the digested food, thereby resulting in higher chemical concentrations in the microplastics. While the model-calibrated kinetic parameters are specific to the studied scenario, we argue that the mechanism of the reduced bioavailability of chemicals and the modeling tool developed have generic relevance. These digestive processes should be considered when assessing the risks of microplastics to humans and also biomagnification in aquatic food webs.

Modeling atmospheric microplastic cycle by GEOS-Chem: An optimized estimation by a global dataset suggests likely 50 times lower ocean emissions

Modeling atmospheric microplastic cycle by GEOS-Chem: An optimized estimation by a global dataset suggests likely 50 times lower ocean emissions

Model of Activated Carbon Dose and Sediment–Water Diffusion Fluxes of Hydrophobic Organic Chemicals: Implications for Sediment Remediation

Activated carbon (AC) amendment is an effective strategy for remediating contaminated sediment by hydrophobic organic chemicals. Reductions of porewater chemical concentrations have been used for estimating recommended AC dose for effective sediment remediation, but the AC dose may have large uncertainties resulting from site-specific parameters. The present study examined sediment–water diffusion flux as an alternative assessment parameter by correlating diffusion fluxes of organophosphorus flame retardants (OPFRs) and polybrominated diphenyl ethers (PBDEs) with AC doses. AC at doses of 8–36% substantially reduced sediment porewater concentrations and diffusion fluxes of the target chemicals. Diffusion fluxes of OPFRs and PBDEs normalized by their corresponding sediment concentrations significantly correlated with total organic carbon contents (r2 = 0.57–0.93). A model was established to estimate the required AC dose for effective sediment amendment from the diffusion flux and sediment concentration of a target chemical. Using contaminated sediment in a typical e-waste recycling zone, the AC doses (0.1 ± 1.3–12.8 ± 0.3%) required to reduce 90% of diffusion fluxes for tri-n-butyl phosphate and BDE-17 were within the recommended range (1.9 ± 3.6–5.6 ± 8.3%) in lowering porewater concentrations by the same magnitude. This finding suggested the feasibility of the new model in supporting sediment remediation.

Incorporating performance reference compounds in retractable/reusable solid phase microextraction fiber for passive sampling of hydrophobic organic contaminants in water

Solid phase microextraction (SPME) has been used to measure aqueous-phase hydrophobic organic chemicals (HOCs) in equilibrium passive sampling mode for over two decades. However, determination of the extent of equilibrium has not been well-established for the retractable/reusable SPME sampler (RR-SPME), especially in the field applications. The goal of this study was to establish a method regarding to sampler preparation and data processing to characterize the extent of equilibrium of HOCs on the RR-SPME (100-μm thickness of polydimethylsiloxane (PDMS) coating) by incorporating performance reference compounds (PRCs). A fast (4 h) PRC loading protocol was identified with using a ternary solvent mixture (i.e., acetone-methanol-water mixture (4:4:2, v/v)) to accommodate diverse carrier solvents of the PRCs. The isotropy of the RR-SPME was validated by a paired, co-exposure approach with 12 different PRCs. The aging factors measured with the co-exposure method approximately equal to one, indicating the isotropic behavior was not changed after storage at 15 °C and −20 °C for 28 days. As a method demonstration, the PRC-loaded RR-SPME samplers were deployed in the ocean off Santa Barbara, CA (USA) for 35 days. The PRCs approaching the extents of equilibrium ranged from 20 ± 15.5 % to 96.5 ± 1.5 % and showed a declining trend along with log KOW increase. A generic equation relationship was deduced based on a correlation relationship of desorption rate constant (k2) and log KOW to extrapolate non-equilibrium correction factor from the PRCs to the HOCs. The merit of the present study is manifested by its theory and implement to enable the RR-SPME passive sampler to be utilized in environmental monitoring.

Influence of water exchange rates on toxicity and bioaccumulation of hydrophobic organic chemicals in sediment toxicity tests.

In standardized sediment toxicity tests, the applied water exchange methods range from static to flow-through conditions and vary between protocols and laboratories even for the same test species. This variation potentially results in variable chemical exposure, hampering the interpretation of toxicity and bioaccumulation. To address these issues, we performed sediment toxicity tests with a mixture of three polycyclic aromatic hydrocarbons (PAHs) and the freshwater epibenthic amphipod Hyalella azteca as model chemicals and organism, respectively. Five standardized water exchange methods were applied: static, semi-static, or flow-through conditions. By measuring total (Cdiss) and freely dissolved concentrations (Cfree) of PAHs with water sampling and direct immersion solid-phase microextraction methods, respectively, we found that Cdiss in overlying water differed by a factor of up to 107 among water exchange conditions, whereas both Cdiss and Cfree in pore water did not differ by more than a factor of 2.6. Similar survival rates, growth rates, and bioaccumulation of PAHs between water exchange methods suggest that H. azteca was predominantly exposed to pore water rather than overlying water. By applying mechanistic kinetic modeling to simulate spatiotemporal concentration profiles in sediment toxicity tests, we discuss the importance of the water exchange rates and resulting temporal and spatial exposure variability for the extrapolation of laboratory sediment toxicity to field conditions, particularly for chemicals with relatively low hydrophobicity and sediments with low organic carbon content.

Adsorption of the hydrophobic organic pollutant hexachlorobenzene to phyllosilicate minerals

Hexachlorobenzene (HCB), a representative of hydrophobic organic chemicals (HOC), belongs to the group of persistent organic pollutants (POPs) that can have harmful effects on humans and other biota. Sorption processes in soils and sediments largely determine the fate of HCB and the risks arising from the compound in the environment. In this context, especially HOC–organic matter interactions are intensively studied, whereas knowledge of HOC adsorption to mineral phases (e.g., clay minerals) is comparatively limited. In this work, we performed batch adsorption experiments of HCB on a set of twelve phyllosilicate mineral sorbents that comprised several smectites, kaolinite, hectorite, chlorite, vermiculite, and illite. The effect of charge and size of exchangeable cations on HCB adsorption was studied using the source clay montmorillonite STx-1b after treatment with nine types of alkali (M+: Li, K, Na, Rb, Cs) and alkaline earth metal cations (M2+: Mg, Ca, Sr, Ba). Molecular modeling simulations based on density functional theory (DFT) calculations to reveal the effect of different cations on the adsorption energy in a selected HCB-clay mineral system accompanied this study. Results for HCB adsorption to minerals showed a large variation of solid–liquid adsorption constants Kd over four orders of magnitude (log Kd 0.9–3.3). Experiments with cation-modified montmorillonite resulted in increasing HCB adsorption with decreasing hydrated radii of exchangeable cations (log Kd 1.3–3.8 for M+ and 1.3–1.4 for M2+). DFT calculations predicted (gas phase) adsorption energies (− 76 to − 24 kJ mol−1 for M+ and − 96 to − 71 kJ mol−1 for M2+) showing a good correlation with Kd values for M2+-modified montmorillonite, whereas a discrepancy was observed for M+-modified montmorillonite. Supported by further calculations, this indicated that the solvent effect plays a relevant role in the adsorption process. Our results provide insight into the influence of minerals on HOC adsorption using HCB as an example and support the relevance of minerals for the environmental fate of HOCs such as for long-term source/sink phenomena in soils and sediments.

Application of equilibrium passive sampling to assess the influence of anthropogenic activities and bioturbation on the distribution of hydrophobic organic chemicals in North Sea sediment cores

The pollution state in the German Bight was investigated by determination of pollutant concentrations of sediment samples using equilibrium passive sampling. Polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAH) were determined in the pore water of North Sea sediment. The freely dissolved pore water concentration (Cfree) was measured applying Solid Phase Microextraction (SPME) by using PDMS-coated glass fibers. The obtained results show that the North Sea contamination level with the investigated pollutants is relatively low. However, the stations close to the sediment-dumping site were higher contaminated. A macrofauna analysis showed that bioturbation activities were mostly present in the upper sediment layers, but a direct bioturbation influence on the sediment concentration distribution could not be shown. Overall, the contamination load was below baseline toxicity, but considering that several other priority pollutants will also make a contribution to the baseline toxicity, it can be counted as relatively high.

Free Versus Bound Concentration: Passive Dosing from Polymer Meshes Elucidates Drivers of Toxicity in Aquatic Tests with Benthic Invertebrates.

Aquatic toxicity tests with benthic organisms are used to predict the toxicity of hydrophobic organic chemicals (HOCs) in sediments, assuming that the freely dissolved concentration (Cfree ) is a good surrogate of bioavailability in the exposure system. However, Cfree of HOCs is difficult to control in water-only setups. Moreover, the role of dissolved organic carbon (DOC) in the occurrence of toxicity needs clarification because DOC concentrations in sediment porewater can be substantially higher than in typical test water. We introduced biocompatible polyethylene meshes with high sorptive capacities and fast release kinetics as a novel passive dosing phase, which maintained Cfree and Cwater (i.e., free + DOC-bound) in Hyalella azteca water-only tests. Adding the supernatant fraction of peat to test water as a DOC source increased Cwater to an extent comparable to sediment porewater and significantly increased and decreased the observed toxicity of permethrin and benzo[a]pyrene, respectively, to H. azteca. This result indicates that DOC can both benefit and harm test species likely due to the increased health after ingestion of DOC and to the uptake of DOC-bound HOCs, respectively. Passive dosing in combination with the addition of sediment DOC surrogates may better reflect exposure and habitat conditions in sediment porewater than conventional aquatic tests. Environ Toxicol Chem 2022;00:1-10. © 2022 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC.

Comparing 10- and 28-Day Sediment Toxicity and Bioaccumulation of Fluoranthene in Hyalella azteca Using Passive Sampling Techniques.

Understanding the changes in the temporal and spatial concentrations of chemical substances in sediment toxicity tests facilitates interpretation of their toxicity and accumulation in benthic organisms because benthic organisms are affected by chemicals via multiple exposure pathways. However, such investigations using chronic sediment toxicity tests have rarely been performed. To examine the concentration profiles of a hydrophobic organic chemical using chronic spiked-sediment toxicity tests, we performed 28-day sediment toxicity tests of fluoranthene with a freshwater amphipod, Hyalella azteca, using a semi-flow-through system and compared the results with those of 10-day tests. In these experiments, we measured various types of fluoranthene concentrations over the test periods: total dissolved (Cdiss ) and freely dissolved (Cfree ) concentrations in overlying water and porewater as well as sediment concentrations. We also examined which concentration correlated with the amphipod bioconcentration factor (BCF). We found that both overlying water and porewater Cfree did not differ significantly on days 10 and 28. Sediment concentrations remained almost stable for 28 days, whereas Cdiss in overlying water varied temporally. These results suggest that the 28-day test provides almost constant concentrations of fluoranthene, particularly in porewater, even in a semi-flow-through system. In addition, the comparison of BCF of fluoranthene on day 10 in the present study with that obtained from water-only tests reported in the literature suggested that Cfree in pore water was the most representative indicator of bioaccumulation in H. azteca. Our findings support the possible use of a water-exchange system in chronic spiked-sediment toxicity tests of hydrophobic organic chemicals. However, further studies using sediments and chemicals with different properties are warranted to generalize the findings of the present study. Environ Toxicol Chem 2022;41:2679-2687. © 2022 SETAC.

Effect of soil pH on the sorption capacity of soil organic matter for polycyclic aromatic hydrocarbons in unsaturated soils

Sorption by soil organic matter (SOM) is considered the most important process affecting the bioavailability of hydrophobic organic chemicals (HOCs) in soils. The sorption capacity of SOM for HOCs is affected by many environmental factors. In this study, we investigated the effects of soil pH on the sorption capacity of SOM using batch sorption experiments. The soil organic carbon-water partition coefficients ( K OC ) of six selected polycyclic aromatic hydrocarbons (PAHs) were measured in artificial soil under various soil pH and water saturation conditions. Passive sampling was used for measurement of K OC with polydimethylsiloxane as sampling material. Regardless of soil pH, K OC increased with increasing soil water saturation for low molecular weight PAHs. On the contrary, K OC decreased with increasing soil water saturation for high molecular weight PAHs. Despite some fluctuations, K OC tended to decrease with increasing soil pH at all water saturations. This indicates that earlier studies on the effects of soil pH on K OC in saturated conditions could be extended to unsaturated soils. These K OC tendencies were reproduced in three different natural soils, suggesting that the effects of water saturation and soil pH might be generalized, at least for PAHs. The sorption capacity of SOM was found to be resilient under dynamic soil pH conditions. The range of sorption capacity of SOM under dynamic soil pH conditions can be used for adjusting the effects of soil pH.

Influence of microplastics on the bioconcentration of organic contaminants in fish: Is the “Trojan horse” effect a matter of concern?

Microplastics (MPs) have been shown to act as sorbent phases and thus carriers of organic chemicals in the aquatic environment. Therefore, concerns exist that MP ingestion increases the uptake and accumulation of organic chemicals by aquatic organisms. However, it is unclear if this pathway is relevant compared to other exposure pathways. Here we compared the bioconcentration capacity of two hydrophobic organic chemicals (i.e., chlorpyrifos and hexachlorobenzene) in a freshwater fish (Danio rerio) when exposed to chemicals through water only and in combination with contaminated polyethylene MPs. Additionally, a suite of biomarker analyses (acetylcholine esterase, glutathione S-transferase, alkaline phosphatase, catalase) was carried out to test whether MPs can enhance the toxic stress caused by chemicals. Two 14-day semi-static experiments (one for each chemical) were carried out with adult fish. Each experiment consisted of (1) a control treatment (no chemicals, no MPs); (2) a treatment in which fish were exposed to chlorpyrifos or hexachlorobenzene only through water; (3) a treatment in which fish were exposed to the chemicals through water and contaminated polyethylene MPs (100 mg MP/L). Two additional treatments were included for the biomarker analysis. These contained MPs at two different concentrations (5 and 100 mg MP/L) but no chemicals. The presence of contaminated MPs in contaminated water did not enhance but rather decreased the bioconcentration of both chemicals in fish compared to the treatment that contained contaminated water in absence of MPs. This was more pronounced for hexachlorobenzene, which is more hydrophobic than chlorpyrifos. Enzyme activity levels in fish were only significantly altered in the presence of MPs for alkaline phosphatase. This study indicates that MP presence in freshwater ecosystems is not expected to increase the risks associated with chemical bioconcentration in aquatic organisms and that other exposure pathways (i.e., uptake via respiration, skin permeability) may be of higher importance.

In-Tube Passive Dosing of Hydrophobic Organic Chemicals: Controlling Freely Dissolved Concentrations in Flow-Through and Large-Volume Experiments

In-Tube Passive Dosing of Hydrophobic Organic Chemicals: Controlling Freely Dissolved Concentrations in Flow-Through and Large-Volume Experiments

PH-Dependent Partitioning of Ionizable Organic Chemicals between the Silicone Polymer Polydimethylsiloxane (PDMS) and Water.

The silicone polymer polydimethysiloxane (PDMS) is a popular passive sampler for in situ and ex situ sampling of hydrophobic organic chemicals. Despite its limited sorptive capacity for polar and ionizable organic chemicals (IOC), IOCs have been found in PDMS when extracting sediment and suspended particulate matter. The pH-dependent partitioning of 190 organics and IOCs covering a range of octanol-water partition constants log K ow from -0.3 to 7.7 was evaluated with a 10-day shaking method using mixtures composed of all chemicals at varying ratios of mass of PDMS to volume of water. This method reproduced the PDMS-water partition constant K PDMS/w of neutral chemicals from the literature and extended the dataset by 93 neutral chemicals. The existing quantitative structure-activity relationship between the log K ow and K PDMS/w could be extended with the measured K PDMS/w linearly to a log K ow of -0.3. Fully charged organics were not taken up into PDMS. Thirty-eight monoprotic organic acids and 42 bases showed negligible uptake of the charged species, and the pH dependence of the apparent D PDMS/w(pH) could be explained by the fraction of neutral species multiplied by the K PDMS/w of the neutral species of these IOCs. Seventeen multiprotic chemicals with up to three acidity constants pK a also showed a pH dependence of D PDMS/w(pH) with the tendency that the neutral and zwitterionic forms showed the highest D PDMS/w(pH). D PDMS/w(pH) of charged species of more hydrophobic multiprotic chemicals such as tetrabromobisphenol A and telmisartan was smaller but not negligible. Since these chemicals show high bioactivity, their contribution to mixture effects has to be considered when testing passive sampling extracts with in vitro bioassays. This work has further implications for understanding the role of microplastic as a vector for organic micropollutants.

Application of Equilibrium Passive Sampling to Assess the Influence of Anthropogenic Activities and Bioturbation on the Distribution of Hydrophobic Organic Chemicals in North Sea Sediment Cores

Application of Equilibrium Passive Sampling to Assess the Influence of Anthropogenic Activities and Bioturbation on the Distribution of Hydrophobic Organic Chemicals in North Sea Sediment Cores

Comparative study on polychlorinated biphenyl sorption to activated carbon and biochar and the influence of natural organic matter

The sorption isotherms of polychlorinated biphenyls (PCBs) on carbons (coal based activated carbon named AC and hardwood derived biochar named BC) and natural organic matter (NOM) loaded carbons were examined and carbon-water partition coefficients (KC-W-PCB) were calculated. The purpose was to accurately predict the effectiveness of in-situ carbon treatments on the sediment impacted with hydrophobic organic chemicals (HOCs). For 1 month sorption, AC KC-W-PCB values were significantly higher than BC, corresponding to the much larger surface area (particularly in mesopores) for AC. BC KC-W-PCB values were correlated with PCB total surface area (TSA) and octanol-water partition coefficient (logKow). After loading with NOM, AC adsorption to PCBs strongly reduced and the fitted Freundlich exponents (n) decreased with increasing NOM level. However, NOM loading slightly impacted BC sorption and exhibited an opposite effect on BC n values. It is illustrated that the sorption mechanisms are different between AC and BC thereby the influences of NOM on sorption characteristics differ vastly. As the sorption time increased from 1 month to 6 months, an increase is observed in BC sorption extent but simultaneously NOM reduction effect on BC sorption increases, implying that more accurately evaluating BC application as an in-situ sorbent amendment for HOC impacted sediment need further investigation. On the contrary, AC adsorption attenuation caused by NOM coating greatly decreases over time, encouraging AC application as a sediment amendment.

Relative Importance of Microplastics as Vectors of Hydrophobic Organic Chemicals to Marine Fish and Seabirds

Relative Importance of Microplastics as Vectors of Hydrophobic Organic Chemicals to Marine Fish and Seabirds