Hydrophobic Organic Compounds Research Articles

Hydrophobic sorption behaviors of 17β-Estradiol on environmental microplastics

Microplastics (MPs) have been regarded as a vector for contaminants and greatly affect the migration and fate of hydrophobic organic compounds (HOCs) in marine water. In this study, the sorption behavior of 17β-estradiol (E2) on MPs was investigated in marine water system. The sorption capacity of E2 varied greatly with the chemical structures of MPs. The adsorption or partition contribution of E2 sorption on MPs was well quantified with adsorption-partition dual-mode model mechanism. The hydrophobic partition dominantly regulates the sorption of E2 due to the high crystallinity of MPs and high accessibility of amorphous domain of rubbery MPs. Smaller particle size benefits the sorption of E2 on same kind of MPs. The salinity and dissolved organic matter (DOM) have minor effect on E2 sorption by MPs in real marine water. The result shows that the MPs greatly influence the transportation of E2 and cause potential environmental risk to marine ecosystem.

Analysis of Non-Ionic Surfactant Triton X-100 Using Hydrophilic Interaction Liquid Chromatography and Mass Spectrometry.

It is well known that surfactants increase the solubility of hydrophobic organic compounds and cause adverse environmental effects. The removal of these compounds from the contaminated soil or ground-water is particularly difficult due to their water soluble feature. In this work, an ultra-high performance hydrophilic interaction liquid chromatographic method was developed for the separation of oligomers of Triton X-100 octylphenol-polyethoxylate non-ionic surfactant. Liquid chromatography-mass spectrometry (LC-MS) was used to identify the Triton X-100 compounds. There was a 44 mass unit difference between two adjacent peaks that is the molar mass of one ethylene oxide group (–CHCHO–). A quadratic retention model was applied for the estimation of retention of the examined non-ionic surfactant and the optimization of gradient elution conditions. The optimized method was suitable for the baseline separation of 28 Triton X-100 oligomers in five minutes.

Substituted naphthalene reaction rates with peroxy-acid treatment: prediction of reactivity using PEST

ABSTRACTPersistent organic contaminants in the environment pose an environmental risk due to widespread occurrence and toxic properties. Advanced oxidation processes (AOPs) are treatment methods that have been used to successfully degrade organic contaminants in water, soil, sediments and sludge. Reaction rate constants (k) for peroxy acid treatment of 10 substituted naphthalene compounds were determined. The treatment method utilized acetic acid, hydrogen peroxide and a sulphuric acid catalyst to degrade the polyaromatic structures found in the compounds. Molecular structures of the selected compounds were derived at the B3LYP/6-31G* level of theory. Property-encoded surface translator (PEST) descriptors were calculated from B3LYP/6-31G* optimized structures and were found to have significant levels of correlation with k. Models using minimum local ionization potential (PIP.MIN) and a histogram [bin] of the gradient of the K electronic kinetic energy normal to the isosurface (DKN) were evaluated and found to agree within 10% of experimentally derived values of k in most instances. Results show that a combination of PEST descriptors could be used to predict reactivity by the peroxy-acid process. The PEST technology could prove to be a valuable asset for effective remediation design by predicting reaction outcomes for substituted naphthalene compounds and possibly other hydrophobic organic compounds (HOCs).

Dietary Uptake Patterns Affect Bioaccumulation and Biomagnification of Hydrophobic Organic Compounds in Fish

Biomagnification of hydrophobic organic compounds (HOCs) increases the eco-environmental risks they pose. Here, we gained mechanistic insights into biomagnification of deuterated polycyclic aromatic hydrocarbons (PAHs- d10) in zebrafish with carefully controlled water (ng L-1) by a passive dosing method and dietary exposures using pre-exposed Daphnia magna and fish food. A new bioaccumulation kinetic model for fish was established to take into account discrete dietary uptake, while the frequently used model regards dietary uptake as a continuous process. We found that when freely dissolved concentrations of the PAHs- d10 were constant in water, the intake amount of the PAHs- d10 played an important role in affecting their steady-state concentrations in zebrafish, and there was a peak concentration in zebrafish after each dietary uptake. Moreover, considering the randomness of predation, the Monte Carlo simulation results showed that the probabilities of biomagnification of the PAHs- d10 in zebrafish increased with their dietary uptake amount and frequency. This study indicates that in addition to the well-known lipid-water partitioning, the bioaccumulation of HOCs in fish is also a discontinuous kinetic process caused by the fluctuation of HOC concentration in the gastrointestinal tract as a result of the discrete food ingestion. The discontinuity and randomness of dietary uptake can partly explain the differences among aquatic ecosystems with respect to biomagnification for species at similar trophic levels and provides new insight for future analysis of experimental and field bioaccumulation data for fish.

Uptake of hydrophobic organic compounds, including organochlorine pesticides, polybrominated diphenyl ethers, and perfluoroalkyl acids in fish and blue crabs of the lower Passaic River, New Jersey, USA.

The bioavailability and bioaccumulation of sedimentary hydrophobic organic compounds (HOCs) is of concern at contaminated sites. Passive samplers have emerged as a promising tool to measure the bioavailability of sedimentary HOCs and possibly to estimate their bioaccumulation. We thus analyzed HOCs including organochlorine pesticides (OCPs), polybrominated diphenyl ethers (PBDEs), polychlorinated biphenyls (PCBs), and polychlorinated dibenzo-p-dioxins/furans (PCDD/Fs) in sediment, porewater, and river water using low-density polyethylene passive samplers and in 11 different finfish species and blue crab from the lower Passaic River. In addition, perfluorinated alkyl acids (PFAAs) were measured in grab water samples, sediment, and fish. Best predictors of bioaccumulation in biota were either porewater concentrations (for PCBs and OCPs) or sediment organic carbon (PBDEs and PFAAs), including black carbon (OCPs, PCBs, and some PCDD/F congeners)-normalized concentrations. Measured lipid-based concentrations of the majority of HOCs exceeded the chemicals' activities in porewater by at least 2-fold, suggesting dietary uptake. Trophic magnification factors were >1 for moderately hydrophobic analytes (log octanol-water partitioning coefficient [KOW ] = 6.5-8.2) with low metabolic transformation rates (<0.01 d-1 ), including longer alkyl chain PFAAs. For analytes with lower (4.5-6.5) and higher (>8.2) KOW s, metabolic transformation was more important in reducing trophic magnification. Environ Toxicol Chem 2019;38:872-882. © 2019 SETAC.

Multifunctional vesicular coacervates as engineered supramolecular solvents for wastewater treatment

In this study, multifunctional supramolecular solvents (SUPRASs) able to simultaneously extract ionic, polar and hydrophobic organic compounds from wastewater have been developed. SUPRASs were synthesized in aqueous solutions containing mixtures of carboxylic acids and carboxylates that underwent spontaneous self-assembly and coacervation under the addition of tetraalkylammonium ions. These SUPRAS consisted of coacervate droplets made up of large unilamellar vesicular aggregates bridged by tetraalkylammonium ions. Both, the high kinetic stability of vesicles and their strong interaction with tetraalkylammonium ions through different bonds working cooperatively, made supramolecular nanostructures in the SUPRAS chemically stable, which minimized the presence of solvent residues in the treated water. The suitability of the synthesized SUPRASs to behave as multifunctional extractants in water treatment was investigated by their application to the removal of anionic, cationic and ionizable dyes and PAHs. All the variables affecting the extraction process were optimized (i.e. chain length of the tetraalkylammonium ion, fractional SUPRAS phase volume, pH, ionic strength, pollutant concentration and stirring time/rate). All the pollutants selected were efficiently removed at room temperature and a fractional SUPRAS phase volume of 0.01. Applicability of the SUPRAS-based treatment to the efficient removal of dyes in textile effluents and benzo(a)pyrene in tap water was proved. Overall, the low cost, easy synthesis and high removal efficiency of these engineered SUPRASs make them highly promising for application in comprehensive wastewater treatments.

Effective removal of Aroclor 1254 and hexachlorobenzene in river sediments by coupling in situ phase-inversion emulsification with biological reductive dechlorination

River sediment contamination is a critical environmental problem. Concentrations of certain hydrophobic organic compounds (HOCs) in sediments in Taiwan are ranked at the top in the world. In this study, we proposed a novel in situ phase-inversion emulsification and biological reductive dechlorination (ISPIE/BiRD) method that integrates (1) heating contaminated sediments by hot water-in-oil emulsion to increase the contact between hydrophobic organic contaminants (HOCs), to accelerate the mass transfer between two phases, and to select heat-tolerant hydrogen-producing bacteria, (2) ISPIE forming oil-in-water emulsion to enhance recovery of HOCs by pushing cool water and nutrient buffer through the sediment column, and (3) subsequent BiRD using residual emulsion in sediment. Aroclor 1254 and hexachlorobenzene (HCB) were selected due to significantly higher human health and ecological risks in sediments. Batch biological dechlorination tests were conducted using an L9(34) orthogonal table according to the Taguchi method. The results showed that significant controlling factors for biological dechlorination were temperature and emulsion concentration. A single operation of ISPIE can achieve the removal of Aroclor 1254 and HCB at as high as 58.2% and 56.5%, respectively. Column study on BiRD further removed about 30% of the residual Aroclor 1254 and HCB at the upper and middle sections of the sediment cores in 35 days. These results supported that ISPIE/BiRD is feasible for HOC-contaminated sediments remediation.

Chasing equilibrium passive sampling of hydrophobic organic compounds in water

We investigated a combination of approaches to extend the attainment of partition equilibria between silicone passive samplers (samplers) and surface or treated waste water towards more hydrophobic organic compounds (HOC). The aim was to identify the HOC hydrophobicity range for which silicone sampler equilibration in water is feasible within a reasonable sampler deployment period. Equilibrium partitioning of HOC between sampler and water is desirable for a simpler application as a “chemometer”, aiming to compare chemical activity gradients across environmental media (e.g. water, sediment, biota). The tested approaches included a) long sampler exposure periods and high water flow to maximize mass transfer from water to sampler; b) the use of samplers with reduced sheet thicknesses; and c) pre-equilibration of samplers with local bottom sediment, followed by their exposure in surface water at the same sampling site. These approaches were tested at three sites including a fish pond with a low level of pollution, a river impacted by an urban agglomeration and an effluent of municipal wastewater treatment plant. Tested compounds included polychlorinated biphenyls (PCB), polycyclic aromatic hydrocarbons (PAH), DDT, its metabolites and their isomers, hexachlorobenzene (HCB) and polybrominated diphenyl ethers (PBDE). The study shows that samplers with a surface area of 400–800 cm2 consisting of thin (100–500 μm) silicone sheets exposed at sampling rates of 10–40 L d−1 for a time period of up to four months reach partition equilibrium with water for compounds with log Kow ≤ 5.5. Nevertheless, for compounds beyond this limit it is challenging, within a reasonable time period, to reach equilibrium between sampler and water in an open system where water boundary layer resistance controls the mass transfer. For more hydrophobic HOC (log Kow > 6), the kinetic method using performance reference compounds is recommended instead.

Liquid-Repellent Metal Oxide Photocatalysts.

Metal oxide photocatalysts (MOPCs) decompose organic molecules under illumination. However, the application of MOPCs in industry and research is currently limited by their intrinsic hydrophilicity because MOPCs can be wetted by most liquids. To achieve liquid repellency, the surface needs to possess a low surface energy, but most organic molecules with low surface energy are degraded by photocatalytic activity. Herein, current methods to achieve liquid repellency on MOPCs, while preventing degradation of hydrophobic coatings, are reviewed. Classically, composite materials containing MOPCs and hydrophobic organic compounds possess good liquid repellency. However, composites normally form irregular coatings and are hard to prepare on surfaces such as those that are mesoporous or nanostructured. In addition, the adhesion of composites to substrates is often weak, resulting in delamination. Recent studies have shown that the direct grafting reaction of polydimethylsiloxane (PDMS) from silicone oil (methyl-terminated PDMS) under illumination results in a stable polymer brush. This easy and simple grafting method allows us to create stable liquid-repellent surfaces on MOPCs of various types, structures, and sizes. In particular, super-liquid-repellent drops with an underlying air layer can be created on PDMS-grafted nano-/microstructured MOPCs. Potential applications of surfaces combining liquid repellency and photocatalytic activity are also discussed; thus offering new ways of using MOPCs in a wider range of applications.

Effects of multi−walled carbon nanotubes on pyrene adsorption and desorption in soils: The role of soil constituents

Once entering soil, carbon nanotubes (CNTs) can influence the fate of hydrophobic organic compounds (HOCs) in soil due to its strong adsorption capacity. This process may be influenced by the interactions between CNTs and soil constituents. The mechanisms therein were investigated in the present study by examining pyrene adsorption/desorption on one CNTs, two soils (black soil and paddy soil), and mixtures thereof. CNTs' amendment enhanced soil site heterogeneity and adsorption capacity of pyrene while it was less than that predicted by the sum of the individual adsorption on soils and CNTs, which was more obvious at low aqueous concentrations. This could be due to the interactions between soil constituents (dissolved organic matter (DOM) and clays) and CNTs. Modification of CNTs by DOM attenuated pyrene adsorption by 14.9%–66.1%, which was ascribed to occupying of surface adsorption sites, pore blockage of CNTs' aggregates, enhancement of surface polarity, and enhancement of pyrene solubility in aqueous phase. The coexistence of clay (kaolinite) also showed inhibition on pyrene adsorption onto CNTs with a reduction of 19.2%−40.2%. This could be ascribed to that the attachment of clay particles on CNTs' aggregates could cover the surface adsorption sites and enhance the surface polarity of CNTs. The effect of CNTs amendment on pyrene desorption hysteresis differed among soils. The hysteresis index of the black soil doubled after CNTs' amendment while that of paddy soil remained unchanged. The results of this study provide insights into the possible effects of CNTs on the fate of HOCs in real soil environment.

Improved biodegradation of hydrophobic volatile organic compounds from the air stream in a multilayer biofilter

Biofiltration of n-hexane as a representative of hydrophobic volatile organic compounds (VOCs) at presence and absence of rhamnolipid biosurfactant was studied using a multilayer biofilter packed with scoria, compost, poplar tree skin and sugar beet pulp, for 131 days. The concentration of n-hexane was measured by a gas chromatograph coupled with a flame ionization detector (GC/FID). The results showed that the mean removal efficiency (RE) of n-hexane at the presence of the biosurfactant was two times higher than that at absence of the biosurfactant. According to the results, rhamnolipid can enhance the efficiency of biofiltration of VOCs from polluted air streams.

Development of predictive models for silicone rubber-water partition coefficients of hydrophobic organic contaminants.

The silicone rubber passive sampling technique is extensively applied to monitor the aqueous freely dissolved concentration of hydrophobic organic compounds (HOCs). The silicone rubber-water partition coefficient (Ksrw) is an important parameter to accurately measure the concentrations of chemicals using passive sampling devices. In this study, two theoretical linear solvation energy relationship (TLSER) models and a quantitative structure-property relationship (QSPR) model were developed for predicting the Ksrw of HOCs. The 119 model compounds studied here included 31 personal care products, such as musks, UV-filters, and organophosphate flame retardants, as well as "conventional" pollutants, such as polycyclic aromatic hydrocarbons and polychlorinated biphenyls. The statistical parameters indicated that the final QSPR model with seven descriptors for all 119 chemicals had a satisfactory goodness-of-fit (Radj2 = 0.898), robustness (QLOO2 = 0.881) and predictive ability (Qext-F1,2,32 = 0.897-0.926). In comparison, the results of one TLSER model with four descriptors for 113 chemicals (Radj2 = 0.826, QLOO2 = 0.790, Qext-F1,2,32 = 0.805-0.837) and another TLSER model with one descriptor for 5 chemicals (Radj2 = 0.747, QLOO2 = 0.647) were also acceptable. The applicability domains of the obtained models covered chemicals containing hydroxyl, imino groups, carbonyl groups, ether bonds, halogen atoms, sulfur atoms, phosphorus atoms, nitro groups, and cyano groups. In addition, the structural features governing the partition behavior of chemicals between silicone rubber and water were explored through interpretation of appropriate mechanisms.

Non-aqueous continuous-flow electrophoresis (NACFE): potential separation complement for continuous-flow organic synthesis

We introduce non-aqueous continuous-flow electrophoresis (NACFE) in which the electrolyte is a solution of an organic salt in an aprotic organic solvent. NACFE can maintain steady-state separation of multiple hydrophobic organic species into individual molecular streams. It is a potential separation complement for continuous-flow organic synthesis. This proof-of-concept work will serve as a justification for efforts towards making NACFE a practical tool in flow chemistry.

Complexation of Iron and Copper in Ambient Particulate Matter and Its Effect on the Oxidative Potential Measured in a Surrogate Lung Fluid.

We investigated the complexation state of atmospheric iron and copper and its impact on the oxidative potential (OP) of ambient PM2.5 (PM, particulate matter). A novel fractionation scheme was developed to segregate three different fractions of Fe and Cu present in ambient PM2.5: (i) complexed with hydrophobic organic compounds, (ii) complexed with hydrophilic organic compounds, and (iii) free or inorganic metal fraction. A solid phase extraction (C-18) column was used to separate these fractions. The fractionation scheme applied to the ambient PM2.5 samples collected from an urban site showed that up to 70-90% of water-soluble Fe and Cu were complexed with the organic compounds. The capability of the complexes of Fe(II) and Cu(II) with Suwanee river fulvic acid (SRFA), a proxy for the atmospheric organic compounds, to generate reactive oxygen species (ROS) (·OH and H2O2) in a surrogate lung fluid (SLF) was measured. The complex of Fe-SRFA showed a strong synergistic effect in the generation of ·OH in SLF, while that of Cu-SRFA showed an additive effect. Overall, our results indicate that organic complexation of the metals in ambient PM could significantly alter their OP and needs to be considered while assessing their health impacts.

Determination of design parameters and cost-effectiveness analysis for a two-liquid phase biofilter treating gaseous dichloromethane

Two-liquid phase biofilter (TLPB) is a new type biofiltration system for controlling hydrophobic volatile organic compounds. In this paper, a mathematical model was developed for a TLPB that can treat gaseous dichloromethane (DCM). The specific growth rate of the biomass inside the TLPB fitted the Monod model. umax and Ks were 0.013 d−1 and 1.288 g m-3, respectively. The Henry’s Law constant of the two liquid phase mixtures was obtained as 0.125 kPa m3 mol−1 under the addition of 10% silicone oil. Simulation results revealed that the model is a good tool for evaluating the removal performance of TLPB. Practical applications of the model indicated that an increase in the silicone-oil-to-mixture ratio and inoculated biomass improved the removal efficiency, whereas an increase in the inlet DCM concentration and gas velocity negatively affected the removal performance. Moreover, the model can be used to determine the design parameters and ensure that the outlet concentration satisfies the emission standards. The results of cost-effectiveness analysis indicated that the expenditure for DCM removal per year was low when TLPB was used to treat a high DCM concentration steam with a long empty-bed retention time.

Passive equilibrium sampling of hydrophobic organic compounds in homogenised fish tissues of low lipid content

Passive equilibrium sampling using polymer samplers in lean tissue is one of the current challenges in assessing bioaccumulation and biomagnification due to the long time needed to reach equilibrium. Despite recent progress achieved by rolling pieces of intact fish fillet with sheets of silicone, there is still a need for a passive sampling method for homogenates that achieves equilibrium before tissue decay starts. In this work, a new approach for relocation of silicone passive samplers in homogenates of lean fish was established for three homogenates with lipid contents varying from 1.2% to 6.1%. Results showed that for 20 model hydrophobic organic compounds with log KOW between 3.9 and 7.8, equilibrium between the silicone and the tissue was achieved in less than 3 days at 4 °C. The concentrations in lipids obtained using passive equilibrium sampling and those from traditional total solvent extraction agreed well, within a factor of 1.3. This new procedure extends the use of passive samplers to homogenised fish tissues of low lipid content, which is highly relevant for environmental studies focused on bioaccumulation of contaminants.

Common flaws in the analysis of river sediments polluted by risk elements and how to avoid them: case study in the Ploučnice River system, Czech Republic

River channel sediments have been widely used to trace current and historical pollution in fluvial systems, although they are not the only media employed for that purpose. The current practice in such use of sediments from sampling strategy, sample pre-treatment and geochemical data processing frequently includes unsubstantiated and redundant steps (e.g., sieving by sub-millimetre meshes) and neglects certain relevant aspects (insufficient attention to what is actually sampled). The aim of this work was to improve that state and to remove redundant steps that make research more time-consuming and potentially introduce biases. The work presents data obtained in the identification of pollution sources in a small catchment with three tributaries (the Ploucnice River, the Czech Republic). The sediments were manually sampled in river channels in sites of recent accumulation of fine solids transported by the river. The samples were pulverised and analysed by X-ray fluorescence spectroscopy. The sediments are composed mostly of silt and sand with most chemical elements, including risk elements “diluted” by quartz and detritic organic matter, which are perfectly suited for geochemical normalization to correctly process compositional data. We avoided statistical tools based on Gaussian distribution, such as means and standard deviations, and instead used median-based statistics better fitting the known properties of geochemical datasets. Sediment sieving to sub-millimetre-size fractions was replaced by geochemical normalization best with Fe and possibly with Rb and Ti, with Al showing implausible performance. The normalization produces grain-size invariant compositional data. The performance of geochemical normalization and downstream variations of risk element concentrations (Pb and Zn) were tested by median-based criteria. Median smoothing of normalized risk element concentrations produced easily interpretable downstream variations of the pollution extent that were independent of grain-size effects and were robust towards the occasional presence of outliers. Channel sediments are suitable for fluvial pollution monitoring if biased routines are avoided. The paper can inspire specialists who plan to perform environmental monitoring and desire to simplify their work and produce robust and unbiased estimates of pollution sources in fluvial systems under anthropogenic pressure. A similar approach could be tested for monitoring of pollution by further elements and hydrophobic organic compounds, except for the need to choose another normalizing element or TOC.

Spatial distribution and source identification of hydrophobic organic compounds (HOCs) on sedimentary microplastic in Hong Kong

The spatial distribution, composition and source of hydrophobic organic compounds (HOCs) including polyaromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs) and organochlorinated pesticides (OCPs) of the sedimentary microplastics (0.25–5 mm) in Hong Kong were investigated. The concentration of ΣPAHs ranged between 70.8 and 1509 ng g−1 with inter-site differences although the regional difference was insignificant, indicating localised pyrolytic and petrogenic input of PAHs. The concentration of ΣPCBs (13–1083 ng g−1) varied with both study sites and regions with higher concentrations obtained in the western waters, possibly due to the input from Pearl River. Significantly higher concentrations of OCPs on eastern shores highlighted fishing and aquaculture activities in South China Sea a potential major source of OCPs. DDT and its metabolites (DDX, ranged from 1.96 to 626 ng g−1) were the dominant forms of OCPs (45%–80%). Since most of the DDX existed as DDT, this suggested that there was a fresh input of DDT into the microplastics. As microplastics and HOCs cannot be removed effectively from the environment, reduction of potential ecotoxicological risks should rely on minimizing the use of plastics and HOCs.

Understanding the mechanisms of soil water repellency from nanoscale to ecosystem scale: a review

Soil water repellency (SWR) can interrupt water infiltration that may decline plant growth and potentially trigger soil erosion. Until now research has been mainly focused on understanding the mechanisms of SWR at different scales by observation and modelling studies. This review systematically discusses the possible mechanisms at different scales of the occurrence and persistence of SWR from nanoscale to ecosystem scale. Soil characteristics are strongly related to the severity of SWR, particularly in soil organic matter and soil moisture. The presence of a higher amount of hydrophobic organic compounds and lower soil moisture content lead to higher water repellency, suggesting that the interaction at the nanoscale between organic compounds and water molecules primarily determines the persistence of SWR. The repeated alternation of drying-wetting process largely modifies the relationship between water molecules and soil particles that impacts the possibility of SWR from hydrophilic in wet condition to hydrophobic in dry condition. Within ecosystem scale, vegetation and microbes are original sources of SWR-inducing compounds influencing the distribution and prevalence of SWR. Nevertheless, the challenge of global climate change, drought and warming can increase SWR. Extreme SWR induces more serious runoff and overland flow that is enhanced by intensive precipitation. We conclude that understanding the interaction of water molecules and organic compounds at soil particle surface is essential to understand SWR at the nanoscale. Expanding the mechanisms of SWR from nanoscale to a larger scale is fundamental to improve the remediation of soil pollution and mitigate global change.

Microplastics in the aquatic environment: Evidence for or against adverse impacts and major knowledge gaps.

There is increasing scientific and public concern over the presence of microplastics in the natural environment. We present the results of a systematic review of the literature to assess the weight of evidence for microplastics causing environmental harm. We conclude that microplastics do occur in surface water and sediments. Fragments and fibers predominate, with beads making up only a small proportion of the detected microplastic types. Concentrations detected are orders of magnitude lower than those reported to affect endpoints such as biochemistry, feeding, reproduction, growth, tissue inflammation and mortality in organisms. The evidence for microplastics acting as a vector for hydrophobic organic compounds to accumulate in organisms is also weak. The available data therefore suggest that these materials are not causing harm to the environment. There is, however, a mismatch between the particle types, size ranges, and concentrations of microplastics used in laboratory tests and those measured in the environment. Select environmental compartments have also received limited attention. There is an urgent need for studies that address this mismatch by performing high quality and more holistic monitoring studies alongside more environmentally realistic effects studies. Only then will we be able to fully characterize risks of microplastics to the environment to support the introduction of regulatory controls that can make a real positive difference to environmental quality. Environ Toxicol Chem 2018;37:2776-2796. © 2018 SETAC.