Previous studies have reported high serum concentrations of polybrominated diphenyl ethers in residents of an electronic waste (e-waste) dismantling site in Guiyu town, South China. In this study, serum levels of Dechlorane Plus (DP), a chlorinated flame retardant of growing concern, were measured in residents of this region, and compared to those of a matched cohort from a nearby region in Haojiang, where fishing is the dominant industry. DP was detected in all the serum samples, with concentrations ranging from 7.8 to 465 ng/g lipid (median: 42.6 ng/g) and 0.93 to 50.5 ng/g lipid (median: 13.7 ng/g) in Guiyu and Haojiang, respectively. The Pearson's correlation coefficient between DP and decabromodiphenyl ether showed a positive relationship in Guiyu (r = 0.931, p < 0.01), but no correlation in Haojiang (r = 0.321, p = 0.34). The average anti-DP fractional abundances (f(anti) ratio) were 0.58 +/- 0.11 and 0.64 +/- 0.05 for Guiyu and Haojiang, respectively (p < 0.01). Tentatively identified dechlorination product ([-Cl + H]) was found in 19/40 serum samples (11/20 for Guiyu, 8/20 for Haojiang). These results suggest that the Guiyu and Haojiang cohorts experienced different dominant exposure routes. It is also possible that DP could bioaccumulate in a stereoselective manner, and undergo dechlorination metabolism. To the best of our knowledge, this is the first study to report DP levels in human serum. Further studies are needed to confirm the results of this study.

Organophosphate esters (OPs) are widely used as flame retardants or plasticizers and are ubiquitously distributed in the environment. In the present study, the occurrence and distribution of 7 widely used OPs were analyzed in sludge samples collected from 19 municipal wastewater treatment plants in the Pearl River Delta, South China. All analytes were detected in these samples, and the total concentration of OPs ranged from 96.7 mg/kg to 1312.9 mg/kg dry weight, with a mean value of 420.1 mg/kg dry weight. In most sludge samples OPs exhibited a similar distribution pattern, for example, tris(2-butoxyethyl) phosphate (TBEP) and triphenyl phosphate (TPhP) were identified as the dominant compounds. However, the results also indicated significantly higher levels of OPs in specific sludges, such as tri-n-butyl phosphate (804.9 mg/kg), TBEP (783.7 mg/kg), TPhP (656.7 mg/kg), and tritolyl phosphate (265.0 mg/kg), which implied different discharge sources in the studied areas.

Previous studies have reported high serum concentrations of polybrominated diphenyl ethers, especially decabromodiphenyl ether (BDE-209), in the residents of an electronic waste (e-waste) dismantling site in Guiyu town, South China. In the present study, human serum samples in this region were collected and pooled for the identification of hydroxylated diphenyl ethers (OH-PBDEs). Three OH-PBDEs, including two hydroxylated octabromodiphenyl ethers (OH-octaBDEs, 6-OH-BDE196 and 6-OH-BDE199) and one hydroxylated nonabromodiphenyl ether (OH-nonaBDE, 6'-OH-BDE206), were first structurally identified. Identification was done by coeluting a mixture of synthetic authentic standards with the methylated OH-PBDEs from the pooled samples using two gas chromatography columns with different polarities. The results were supported by full scan mass spectrometric data in electron capture negative ionization mode. All three OH-PBDE metabolites had hydroxy groups substituted in the ortho position. These results indicate that hydroxylated higher brominated diphenyl ethers such as OH-octaBDEs and OH-nonaBDEs can accumulate in human blood. The results suggest that higher brominated diphenyl ethers could be oxidatively metabolized into OH-PBDEs in humans. Because low brominated OH-PBDEs can also be detected in abiotic media, further investigations are needed to determine the presence of higher brominated OH-PBDEs in the environment in this region.

A facile micro/nano-bubble method was firstly applied to synthesize an Au/TiO2@CNT composite photocatalyst for photocatalytic degradation of gaseous styrene.

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Volatiles of six sweet orange essential oils with different origins were characterized by descriptive sensory analysis, gas chromatography‐mass spectrometry (GC‐MS) and gas chromatography‐olfactometry (GC‐O). Six attributes (green, fruity, peely, fatty, floral and wood) were selected to assess sweet orange essential oils, in which 64 volatile compounds were detected by GC‐MS. Monoterpenes constituted the largest chemical group among the volatiles of the essential oils. Thirty‐one aroma compounds having more than a 50% detection frequency and large span were selected as major odour active compounds correlated with sensory evaluation assessed by partial least squares regression (PLSR). The correlation result showed α‐pinene, sabinene, limonene, δ‐terpinolene, hexanal, octanal, decanal and dodecanal were typical aroma compounds, which co‐varied with a characteristic aroma of the sweet orange essential oil. Copyright © 2015 John Wiley & Sons, Ltd.

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