Organophosphate esters and synthetic musks in the sediments of the Yangtze River Estuary and adjacent East China Sea: Occurrence, distribution, and potential ecological risks.

Occurrence, distribution, and potential ecological risks of ten organophosphate esters (OPEs) and nine synthetic musks (SMs) were investigated in sediments from the Yangtze River Estuary (YRE) and adjacent East China Sea (ECS). The total concentrations of OPEs in the surface sediments ranged from 0.977 to 19.0 ng/g dry weight (dw) with tris(2-chloro-propyl) phosphate being the dominant component. Total concentrations of SMs ranged from 0.176 to 7.25 ng/g dw, with 1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran and 7-acetyl-1,1,3,4,4,6-hexamethyl-1,2,3,4-tetrahydronaphthalene as the dominant SMs. Higher sedimentary concentrations of ΣOPEs and ΣSMs were found in the river mouths of the YRE, inter face of Hangzhou Bay, and mud area of the ECS; the results suggested that terrestrial discharge might be the main source of OPEs and SMs in the studied region. Risk assessment revealed that low ecological risks were posed by OPEs, and limited to low ecological risks were posed by SMs.

Occurrence, congener patterns, and potential ecological risk of chlorinated paraffins in sediments of Yangtze River Estuary and adjacent East China Sea.

Chlorinated paraffins (CPs) are high production volume chemicals with immense scientific research interest due to their wide distribution, persistence, toxicity, and bioaccumulation potential. In this study, 87 surface sediments were collected from the Yangtze River Estuary (YRE) and the adjacent East China Sea (ECS). We investigated the concentrations, spatial distribution, and composition profiles of short-chain chlorinated paraffins (SCCPs) and medium-chain chlorinated paraffins (MCCPs) using ultra-high-performance liquid chromatography coupled with Orbitrap Fusion Tribrid mass spectrometry. The sedimentary concentrations of SCCPs and MCCPs ranged from 2.85 to 94.7 ng·g-1 (median 13.7 ng·g-1) and 3.33 to 77.8 ng·g-1 (median 13.3 ng·g-1), respectively. Higher CP concentrations were found in YRE sediments. The values decreased away from the location, implying a direct influence of the Yangtze River. The SCCP concentrations were higher than those of MCCPs in most sediment samples. Overall, the predominant homologs were C13Cl5-7 and C14Cl6-8 for MCCPs and SCCPs, respectively. Overall, the sediment-dwelling organisms in the region are susceptible to low ecological risks.

Occurrence of short- and medium-chain chlorinated paraffins in soils and sediments from Dongguan City, South China.

As a group of emerging organic pollutants, chlorinated paraffins (CPs) have attracted rising global attention due to their persistence and toxicity. In this study, we have investigated the concentration levels and profiles of short-chain chlorinated paraffins (SCCPs) and medium-chain chlorinated paraffins (MCCPs) in soils and sediments from Dongguan City, an industrial area in South China, and have also screened very short-chain chlorinated paraffins (vSCCPs) by means of ultra-high resolution liquid chromatograph coupled with an Orbitrap Fusion Tribrid mass spectrometer. The results indicated that total SCCP concentrations ranged from 6.75 to 993 ng/g (mean 172 ng/g) in soils and from 4.00 to 613 ng/g (mean 153 ng/g) in sediments, respectively. Higher MCCP levels were observed with a range of 23.9-2427 ng/g (mean 369 ng/g) in soils and 14.0-1581 ng/g (mean 493 ng/g) in sediments, respectively. The results indicated that MCCPs dominated over SCCPs in the studied region. The dominant homologues in soils and sediments were C13Cl6-7 and C14Cl7-8, C13Cl7, and C14Cl7-8, respectively. Furthermore, six vSCCP homologues (C8Cl7-8 and C9Cl5-8) in soils and four vSCCPs (C9Cl5-8) in sediments have been identified. Because of their higher detection frequencies, further studies should focus on the transformation mechanisms and toxicities of these vSCCPs in environmental media and biota.

The quantification of chlorinated paraffins in environmental samples by ultra-high-performance liquid chromatography coupled with Orbitrap Fusion Tribrid mass spectrometry.

As high-production-volume chemicals, chlorinated paraffins (CPs) have raised an increasing environmental concern in recent years. However, their accurate analysis and quantification is still a huge challenge due to the high complexity of their technical formulations and the interference from CPs congeners and other polychlorinated products. In this study, a novel method for the simultaneous analysis of short-chain (SC) and medium-chain (MC) CPs in a single injection has been developed using ultra-high-performance liquid chromatography coupled with Orbitrap Fusion Tribrid mass spectrometry (UHPLC-Orbitrap Fusion TMS). Compared with other analytical methods for CPs, this novel method can greatly shorten the measurement time and provides a lower limit of detection. A high resolution of 120,000 FWHM was set to avoid the self-interference of CPs congeners and to eliminate interferences from chlorinated olefins (COs). Accuracies for SCCPs and MCCPs standards were evaluated at 75-103% and 83-118%, respectively. The developed method was further validated by determining CPs in sediment, soil, and indoor dust samples. This novel method gives higher CPs concentrations than those achieved by gas chromatography-electron capture negative ionization low-resolution mass spectrometry (GC-ECNI-LRMS), with factors of 1.1-12.5 for SCCPs and 0.7-2.7 for MCCPs, respectively. Some new CPs, such as C8Cl7-8 and C9Cl5-8, have been determined in soil samples for the first time, indicating great potential of this novel method for routine CP analysis in various environmental samples.

A full-scale study on thermal degradation of polychlorinated dibenzo- p-dioxins and dibenzofurans in municipal solid waste incinerator fly ash and its secondary air pollution control in China.

Degradation of polychlorinated dibenzo- p-dioxins and dibenzofurans in municipal solid waste incinerator fly ash is beneficial to its risk control. Fly ash was treated in a full-scale thermal degradation system (capacity 1 t d-1) to remove polychlorinated dibenzo- p-dioxins and dibenzofurans. Apart from the confirmation of the polychlorinated dibenzo- p-dioxin and dibenzofuran decomposition efficiency, we focused on two major issues that are the major obstacles for commercialising this decomposition technology in China, desorption and regeneration of dioxins and control of secondary air pollution. The toxic equivalent quantity values of polychlorinated dibenzo- p-dioxins and dibenzofurans decreased to <6 ng kg-1 and the detoxification rate was ⩾97% after treatment for 1 h at 400 °C under oxygen-deficient conditions. About 8.49% of the polychlorinated dibenzo- p-dioxins and dibenzofurans in toxic equivalent quantity (TEQ) of the original fly ash were desorbed or regenerated. The extreme high polychlorinated dibenzo- p-dioxin and dibenzofuran levels and dibenzo- p-dioxin and dibenzofuran congener profiles in the dust of the flue gas showed that desorption was the main reason, rather than de novo synthesis of polychlorinated dibenzo- p-dioxins and dibenzofurans in the exhaust pipe. Degradation furnace flue gas was introduced to the municipal solid waste incinerator economiser, and then co-processed in the air pollution control system. The degradation furnace released relatively large amounts of cadmium, lead and polychlorinated dibenzo- p-dioxins and dibenzofurans compared with the municipal solid waste incinerator, but the amounts emitted to the atmosphere did not exceed the Chinese national emission limits. Thermal degradation can therefore be used as a polychlorinated dibenzo- p-dioxin and dibenzofuran abatement method for municipal solid waste incinerator source in China.

Thermal dechlorination of heavily PCB-contaminated soils from a sealed site of PCB-containing electrical equipment.

A large amount of soils are contaminated by leakage of polychlorinated biphenyls (PCBs) from sealed-up PCB-containing electrical equipment in China. Thermal dechlorination of soils contaminated with PCBs at a level of 108 mg g(-1) and PCB77 (3,3',4,4'-tetrachlorobiphenyl) as a model isomer in conjunction with calcium oxide was investigated in this study. The PCB dechlorination rate improved with increased temperature and time. The highest dechlorination rate was 85.3 %, and temperature was the main influencing factor. Pentachlorobiphenyl and tetrachlorobiphenyl in soils decreased or disappeared in response to treatment at 350 and 400 °C for 4 h, while monochlorinated biphenyl and biphenyl were detected after the reaction, indicating the presence of a dechlorination/hydrogenation pathway. Discrepancy in chlorine balance was observed after low-temperature thermal dechlorination. The species of dechlorination products were identified as amorphous carbon containing a crystalline graphite plane structure and a carbonyl group-containing polymerized product, demonstrating the existence of a dechlorination/polymerization pathway. The yield of amorphous carbon and high-molecular-weight intermediates increased with heating time. The results showed that the discrepancy in chlorine balance was because of the generation of polymerized products and undetected intermediates.