Enhanced Emission from WSe2 Monolayers Coupled to Circular Bragg Gratings

Two-dimensional transition-metal dichalcogenides (TMDC) are of great interest for on-chip nanophotonics due to their unique optoelectronic properties. Here, we propose and realize coupling of tungsten diselenide (WSe2) monolayers to circular Bragg grating structures to achieve enhanced emission. The interaction between WSe2 and the resonant mode of the structure results in Purcell-enhanced emission, while the symmetric geometrical structure improves the directionality of the out-coupling stream of emitted photons. Furthermore, this hybrid structure produces a record high contrast of the spin valley readout (> 40%) revealed by the polarization resolved photoluminescence (PL) measurements. Our results are promising for on-chip integration of TMDC monolayers with optical resonators for nanophotonic circuits

Determination and Source Apportionment of Five Classes of Steroid Hormones in Urban Rivers

We developed an original analytical method for monitoring five estrogens, nine androgens, nine progestogens, six glucocorticoids, and one mineralocorticoid in one water sample using liquid chromatography-electrospray tandem mass spectrometry, and then 45 river, 13 discharging sites, and 4 composite effluent samples were analyzed to reveal their occurrence and sources in urban rivers. Of the 45 river samples, androgens were the dominant steroids detected (total concentrations up to 480 ng/L), followed by glucocorticoids (up to 52 ng/L), progestogens (up to 50 ng/L), and estrogens (up to 9.8 ng/L). The summed concentration for each class of detected hormones in 13 discharging site samples was higher than that in river samples, up to 1887 ng/L for androgens, 390 ng/L for glucocorticoids, 75 ng/L for progestogens, and 25 ng/L for estrogens. A principal component analyses with multiple linear regression based on the profiles of all target compounds was applied to identify the source apportionment and to predict the contribution from different sources. It was found that 62.7% of the mean summed hormones were contributed by freshly discharged untreated sewage, 29.4% by treated sewage and/or naturally attenuated untreated sewage, and 7.9% by an unknown source, possibly pharmaceutical manufacturing plants

Trophic Dilution of Polycyclic Aromatic Hydrocarbons (PAHs) in a Marine Food Web from Bohai Bay, North China

Trophic transfer of polycyclic aromatic hydrocarbons (PAHs) in aquatic ecosystems is an important criterion for assessing their ecological risk. This study analyzed 18 PAHs in phytoplankton/seston, zooplankton, five invertebrate species, five fish species, and one seabird species collected from Bohai Bay, and trophic transfer of the PAHs was determined in the food web, of which the length was approximately 4 on the basis of stable nitrogen isotope values. The concentrations of PAHs (2−64.5 ng/g wet weight) in the marine ecosystem were moderate compared with other marine organisms worldwide, and the PAH compositions exhibited species-specific profiles that were related to trophic levels in some organisms. Significant negative relationships were also found between trophic levels and lipid-normalized concentrations for 10 PAH compounds (acenaphthylene, anthracene, fluoranthene, pyrene, chrysene, benz[a]anthracene, benzo[b]fluoranthene + benzo[k]fluoranthene, benzo[e]pyrene, benzo[a]pyrene, and perylene), and their trophic magnification factors (TMFs) ranged from 0.11 for fluoranthene to 0.45 for acenaphthylene. These results confirm that PAHs undergo trophic dilution in the marine food web, which is likely to be the combined results of low assimilation efficiencies and efficient metabolic transformation at higher trophic levels

Derivatization for Nontargeted Screening of Acids in Oilfield Refinery Wastewater: Identification and Behaviors of Recalcitrant Chlorinated Naphthenic Acids

The nontargeted scanning chemical profiling approach has shown great potential to identify unknown pollutants or novel biological markers; however, the structure identification of unknown compounds is a challenge. In this study, a carboxyl-specific derivatization reagent, N-(4-aminomethylphenyl) pyridinium (AMPP), was coupled with QTOF–MSE–MS scanning to establish a high-throughput nontargeted scanning method for acid compounds. The scanning method can isolate the precursor by data-independent acquisition and can select all of the acid compounds based on the characteristic fragment generated from the derivatization reagent. The method was applied to scan naphthenic acid fraction compounds in petroleum refinery wastewater and identify 70–126 NAs, 30–68 oxy-NAs, 54–60 NAs containing nitrogen, and 66–75 NAs containing both nitrogen and oxygen. Chlorinated NAs (Cl-NAs) including monochlorinated NAs (Cl-NAs), monochlorinated hydroxylated NAs (Cl–OH-NAs), and dichlorinated dihydroxylated NAs (Cl2-(OH)2-NAs) were first identified with the aid of chlorine isotopic patterns. The Cl-NAs might be naturally presented in crude oil together with NAs. Occurrences and mass balances of Cl-NAs were further assessed in the wastewater treatment plant in north China. The total concentrations of ∑Cl-NAs were estimated to be 12 ± 7.8–18 ± 17 μg/L and 8.5 ± 2.0–68 ± 35 μg/g in the wastewater and solid samples, respectively. The removal efficiencies of Cl-NAs (−29.9 to 34.3%) were much lower than those of NAs, suggesting the high recalcitrance of chlorinated compounds during the treatment processes. The estimated mass loss fractions due to degradation for Cl-NAs were 26.5–53.4% of initial loadings, and relatively high fractions (32.1–56.8%) were observed in the effluent directly discharged to the environment. Advanced treatment techniques are needed to effectively reduce the persistent Cl-NAs in the wastewater

A stochastic modelling framework for predicting flexural properties of ultra-thin randomly oriented strands

A stochastic modelling framework is developed to predict the flexural properties of high-strength sheet moulding compounds made of randomly oriented ultra-thin carbon fibre-reinforced thermoplastic prepreg tapes. The model enables reliable designs using ultra-thin randomly oriented strands with less testing, leading to potential applications in automotive primary structures. The stochastic model is based on a Monte Carlo simulation. The flexural modulus is predicted using classical laminate theory, while the flexural strength is predicted by following a Weibull distribution. Fibre discontinuities are considered through stress concentrations introduced by tape overlaps. The results are validated against new 3-point bending and previously reported 4-point bending experimental results. A scaling effect on strength and scatter is predicted, and its implications for structural applications are also discussed. </p

Trophodynamics of Polybrominated Diphenyl Ethers in the Marine Food Web of Bohai Bay, North China

Polybrominated diphenyl ethers (PBDEs) are of great environmental concern due to the exponential increase of the concentrations in the environment, especially in high trophic level organisms, and the trophodynamics of these chemicals in aquatic food webs is an important criterion for assessing their ecological risk. This study analyzed 13 PBDEs in the zooplankton, five invertebrate species, six fish species, and one marine bird species collected from Bohai Bay. PBDE concentrations in organisms from Bohai Bay (ΣPBDEs: 0.15–32.8 ng/g lipid weight) were low compared with other marine organisms worldwide, and BDE-47 was the predominant compound in most samples, followed by BDE-28, BDE-99/BDE-100, and BDE-119. Correlation between lipid-normalized concentrations of PBDEs, and trophic levels determined by stable nitrogen isotope technologies confirmed that PBDEs were biomagnified in the marine food web. Significantly positive relationships were found for total PBDEs and four PBDE compounds (BDE-28, BDE-47, BDE-100, and BDE-119), and their trophic magnification factors (TMFs) were 3.53, 3.57, 7.24, 3.23, and 2.60, respectively. The concentration ratios between congeners (BDE-99/BDE-100 and BDE-99/BDE-47) were found to decrease with increasing trophic levels, suggesting that trophic-level-dependent concentrations ratios between BDE-99 and BDE-100 would be contributed by trophic level-dependent biotransformation between BDE-99 and BDE-47, and therefore resulting in the dominance of BDE-100 compared with BDE-99 and the relatively high trophic magnification of BDE-47 in the marine food web

Visualized Networking of Co-Regulated Lipids in Human Blood Based on High-Throughput Screening Data: Implications for Exposure Assessment

Exposure to environmental chemicals could disturb lipidome homeostasis in biotas. Comprehensive identification and interpretation of lipid molecules in biological samples are of great importance to elucidate the potential changes in lipid homeostasis upon exposure to various environmental stimuli. In this study, a total of 156 human blood samples were collected including 108 general citizens (control group) and 48 employees in a municipal solid waste incineration (MSWI) plant (occupational exposure group). More than 1500 lipid molecules, belonging to five lipid classes, were screened in the blood samples by UPLC-QTOF–MS in the MSE acquisition mode. All of the coupled compounds with correlation coefficients (R) of 0.7 or higher were selected for automated network correlation analysis. A global visual network was automatically produced from thousands of coregulated lipid species in the blood samples. In the automatically produced molecular network, the distributions of the major correlated lipids were in accordance with their metabolic pathways in the KEGG map. Different lipidomic profiles in the blood samples from the two groups of people were easily observed by this visualization technique. Among the intrinsic lipid classes, glycererides and sterol lipids might represent the most sensitively affected lipids upon exposure to various pollutants emitted from the MSWI plant. The visualized network of coregulated lipids identified in human blood presents a new approach for interpreting the metabolic relationships among the thousands of metabolites identified in toxicological and epidemiological studies

Isomer-Specific Trophic Transfer of Perfluorocarboxylic Acids in the Marine Food Web of Liaodong Bay, North China

Trophic transfers of perfluorocarboxylic acids (PFCAs) have been well studied in aquatic food webs; however, most studies examined PFCAs as single compounds without differentiating isomers. In this study, an in-port derivatization GC-MS method was used to determine PFCA (perfluorooctanoic acid, PFOA; perfluorononanoic acid, PFNA; perfluorodecanoate acid, PFDA; perfluoroundecanoate acid, PFUnDA; perfluorododecanoate acid, PFDoDA; perfluorotridecanoate acid, PFTriDA, and perfluorotetradecanoate acid, PFTeDA) structural isomers in 11 marine species including benthic invertebrates, fishes, and gulls collected in November 2006 from Liaodong Bay in China. The total concentrations of linear PFCAs were 0.35–1.10, 0.93–2.61, and 2.13–2.69 ng/g ww, and the corresponding percentages of branched PFCAs to linear PFCAs were 6.6–15.5%, 4.2–9.9%, and 4.5–6.0% in invertebrates, fishes, and birds, respectively. Except for linear PFOA, significant positive relationships were found between the concentrations of all the target linear PFCAs and trophic levels, and the trophic magnification factors (TMFs) ranged from 1.90 to 4.88. Positive correlations between the concentrations of branched PFCAs isomers and trophic levels were also observed but were without statistical significance. The relatively high biomagnification of linear isomers of PFCAs would lead to low percentages of branched PFCAs to total PFCAs in organisms at high trophic levels. This study for the first time clarified isomer-specific trophic transfers of PFCAs in a marine food web

Distribution is a Major Factor Affecting Bioaccumulation of Decabrominated Diphenyl Ether: Chinese Sturgeon (<i>Acipenser sinensis</i>) as an Example

While decabromodiphenyl ether (BDE-209) has very low bioavailability and a rapid biotransformation rate, it exhibits high bioaccumulation in wildlife. To explore the bioaccumulation mechanism of BDE-209 in organisms, its toxicokinetic processes were investigated in Chinese sturgeons from the Yangtze River. Different from less brominated BDEs, lipids did not play an important role in the distribution of BDE-209 with relatively high concentrations detected in liver (54.5 ± 3.3 ng/g wet weight (ww)), gills (47.4 ± 2.9 ng/g ww), and intestine (41.9 ± 3.0 ng/g ww), followed by stomach (21.9 ± 9.0 ng/g ww), muscle (19.1 ± 5.6 ng/g ww), heart (7.5 ± 5.2 ng/g ww), gonad (6.8 ± 4.9 ng/g ww), adipose (4.9 ± 1.2 ng/g ww), and egg (2.8 ± 2.3 ng/g ww). In vitro metabolism of BDE-209 by microsomal fractions of Chinese sturgeon found that BDE-209 was biotransformed rapidly with the rate constant (<i>K</i>) of 0.039 h^–1 in liver. BDE-126, BDE-154, BDE-188, BDE-184, BDE-183, BDE-202, BDE-201, and BDE-204/197 were observed as debrominated products of BDE-209 after incubation, and their formation rates were 0.026, 0.016, and 0.006 h^–1 for BDE-126 BDE-184, and BDE-154, respectively. The concentration ratios between heart and intestine for individual PBDEs suggested slow delivery of BDE-209 among tissues after absorption. A Bayesian hierarchical model was further developed to estimate partition coefficients in a physiologically based pharmacokinetic model of BDE-209 in Chinese sturgeon. The estimated partition coefficients between tissues and blood were higher than those of less brominated BDE or PCBs in various animals, suggesting that the low partition ratios from blood to tissues would lead to high bioaccumulation of BDE-209, especially in absorbing organs