SwePub
Sök i SwePub databas

  Extended search

Träfflista för sökning "WFRF:(Jiang Guibin) "

Search: WFRF:(Jiang Guibin)

  • Result 1-50 of 100
Sort/group result
   
EnumerationReferenceCoverFind
1.
  • Chen, Baowei, et al. (author)
  • Methylation mechanism of tin(II) by methylcobalamin in aquatic systems
  • 2007
  • In: Chemosphere. - : Elsevier BV. - 0045-6535 .- 1879-1298. ; 68:3, s. 414-419
  • Journal article (peer-reviewed)abstract
    • The methylation reaction of tin(II) with methylcobalamin (CH(3)B(12)) in aquatic systems was modeled in the laboratory. The products were detected by a sensitive gas chromatography-flame photometric detector (GC-FPD), and further identified by gas chromatography-mass spectrometry (GC-MS). Both monomethyltin (MMT) and dimethyltin (DMT) were found as methylation products. Three important effecting factors during the methylation reaction, salinity, pH and aerobic or anaerobic, were studied. The results showed that methyl group can be transferred from CH(3)B(12) to tin in aquatic solutions as a radical or carbonium, as well as a carbanion. Two explanations for the pH-dependency of the methylation reaction between tin(II) and CH(3)B(12) were proposed: pH-dependency of the equilibrium states of CH(3)B(12), and pH-dependency of inorganic tin(II) species whose reactivity vary with the redox potential in the solution. Salinity can influence the activity of the methyl donor, which cause changes in the methylation efficiency. Kinetic experiments showed that the methylation reaction was pseudo-first-order for CH(3)B(12).
  •  
2.
  • Chen, Baowei, et al. (author)
  • Methylation of inorganic mercury by methylcobalamin in aquatic systems
  • 2007
  • In: Applied organometallic chemistry. - : John Wiley & Sons. - 0268-2605 .- 1099-0739. ; 21:6, s. 462-467
  • Journal article (peer-reviewed)abstract
    • The methylation of inorganic Hg(II) by methylcobalamin in aquatic systems was studied using high-performance liquid chromatography coupled with UV-digestion cold vapor atomic fluorescence spectrometry (HPLC-UV-CV AFS). Monomethylmercury (MMC) could be positively identified as the reaction product in the aqueous solution. The salinity and pH of the aquatic system have great effects on the formation of MMC, because they could change the species of the reactants in the solution. From an electrophile reaction point of view, salinity and pH alter the electron density of the methyl donor and the electrophilicity of metal ion in the reaction system. This methylation of inorganic Hg(II) is shown to be possible even in highly saline solutions, which indicates its importance in aquatic environments. Kinetic experiments showed that the methylation reaction was fast and first-order for Hg(II). The first-order reaction rate was determined to be 0.00612 and 0.000287 min-1 for pH 5.0 and 1.5, respectively. It is suggested that this methylation could occur in the absence of enzymes, in which Hg(II) acts as an electrophile to attack methylcobalamin with a subsequent transfer of carbanion methyl group to the higher oxidized state of Hg(II).
  •  
3.
  • Chen, Baowei, et al. (author)
  • Simulate methylation reaction of arsenic(III) with methyl iodide in an aquatic system
  • 2006
  • In: Applied organometallic chemistry. - : John Wiley & Sons. - 0268-2605 .- 1099-0739. ; 20:11, s. 747-753
  • Journal article (peer-reviewed)abstract
    • The methylation reaction of inorganic arsenic occurring in aquatic systems was studied by HPLC-HGAFS as a method to separate and detect soluble methylarsenic species. Transformation from inorganic arsenic to methylarsenic was essential for major changes in toxicity to organisms. Monomethylarsenic [AsOCH(3)(OH)(2)] was the only product in the methylation reaction of inorganic arsenic(III) with methyl iodide (MeI). This process can be described as an oxidative carbonium-ion transfer, with MeI acting as a methyl donor. From a thermodynamic point of view, the activity of the carbonium ion and pH were the two major influencing factors. The pH dependence of redox potential of As(III) was the reason for the effect of pH on methylation of arsenic. The influences of salinity and concentration of the methyl donor may be explained by their effects on the activity of carbonium. Moreover, kinetics experiments demonstrated that the methylation reaction was first-order for both As(III) and methyl iodide. First-order reaction rates were also calculated at different pH, salinity and MeI, and were found to be in the range 0.0026-0.0123 h(-1). The methylation rate varied largely under different reaction conditions.
  •  
4.
  • Fu, Jianjie, et al. (author)
  • Elevated levels of perfluoroalkyl acids in family members of occupationally exposed workers : the importance of dust transfer
  • 2015
  • In: Scientific Reports. - : Nature Publishing Group. - 2045-2322. ; 5
  • Journal article (peer-reviewed)abstract
    • The exposure pathways of perfluoroalkyl acids (PFAAs) to humans are still not clear because of the complex living environment, and few studies have simultaneously investigated the bioaccumulative behaviour of different PFAAs in humans. In this study, serum, dust, duplicate diet, and other matrices were collected around a manufacturing plant in China, and homologous series of PFAAs were analysed. PFAA levels in dust and serum of local residents in this area were considerably higher than those in non-polluted area. Although dietary intake was the major exposure pathway in the present study, dust ingestion played an important role in this case. Serum PFAAs in local residents was significantly correlated with dust PFAAs levels in their living or working microenvironment. Serum PFAAs and dust PFAAs were significantly higher in family members of occupational workers (FM) than in ordinary residents (OR) (p<0.01). After a careful analysis of the PFAAs exposure pathway, a potential pathway in addition to direct dust ingestion was suggested: PFAAs might transferred from occupational worker's clothes to dinners via cooking processes. The bioaccumulative potential of PFHxS and PFOS were higher than other PFAAs, which suggested a substantial difference between the bioaccumulative ability of perfluorinated sulfonic acids and perfluorinated carboxylic acids.
  •  
5.
  • Fu, Jianjie, et al. (author)
  • High levels of heavy metals in rice (Oryza sativa L.) from a typical E-waste recycling area in southeast China and its potential risk to human health
  • 2008
  • In: Chemosphere. - : Elsevier BV. - 0045-6535 .- 1879-1298. ; 71:7, s. 1269-1275
  • Journal article (peer-reviewed)abstract
    • Very few studies have investigated the heavy metal contents in rice samples from a typical E-waste recycling area. In this study, 10 heavy metals (As, Ba, Cd, Co, Cr, Cu, Hg, Mn, Ni and Pb) in 13 polished rice and relevant hull samples, six relevant paddy soil samples were investigated. The geometric mean concentrations of Cd, Cu and Hg in soil samples were 1.19, 9.98 and 0.32 microg g(-1), respectively, which were 4.0, 2.0 and 1.1-folds of the maximum allowable concentration (MAC) (0.30, 50.00, 0.30 microg g(-1), respectively) for Chinese agricultural soils. The analyzed metal concentrations were significantly different between rice and relevant hull except for As, Cd and Hg (p<0.05). All metal concentrations, except for Co, in rice hull were higher than those in polished rice. The geometric mean of Pb in polished rice reached 0.69 microg g(-1), which was 3.5-folds higher than the MAC (0.20 microg g(-1)) by the safety criteria for milled rice. Cd contents in 31% of the rice samples exceeded the national MAC (0.20 microg g(-1)), and the arithmetic mean also slightly exceeded national MAC. In addition, Cd and Pb contents in local rice were much higher than commercial rice samples examined in this work and previous studies. Comparing the tolerable daily intakes given by FAO/WHO with the mean estimated daily intakes; Pb daily intake through rice consumption in this area was 3.7 microg day(-1)kg(-1) body weight (bw), which already exceeded the FAO tolerable daily intake, and the Cd daily intake (0.7 microg day(-1)kg(-1) bw) through rice had already taken up 70% of the total tolerable daily intake (1 microg day(-1)kg(-1) bw). The daily intake of Hg and As through rice was much lower than the tolerable daily intakes, but bioaccumulation of Hg through the food chain and intake of As from other food stuff should also be of concern.
  •  
6.
  • Fu, Jianjie, et al. (author)
  • Influence of e-waste dismantling and its regulations : temporal trend, spatial distribution of heavy metals in rice grains, and its potential health risk
  • 2013
  • In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 47:13, s. 7437-7445
  • Journal article (peer-reviewed)abstract
    • Enhanced regulations, centralized dismantling processes, and sophisticated recycling technologies have been implemented in some e-waste dismantling areas in China with regard to environmental and economic aspects since 2005. In this study, rice grain samples were collected from 2006 to 2010 in an e-waste dismantling area to investigate the temporal trends and spatial distribution of As, Cd, Cu, and Pb. Geometric means of As, Cd, Cu, and Pb in rice samples from the e-waste dismantling area were 111, 217, 4676, and 237 ng g(-1), respectively. Levels of Pb showed a significant decreasing trend during the sampling period, whereas the other three elements remained relatively constant or even increased. Concentrations of Cd, Cu, and Pb in the e-waste dismantling area were significantly higher than those in the non-e-waste dismantling area (p < 0.05), which showed a close connection between e-waste dismantling activities and elevated Pb, Cu, and Cd contents. Risk assessment for human via rice consumption indicated that over 60% of the hazard quotient of Cd exceeded 1 in the e-waste dismantling area. Our study implied that stricter implementation of regulatory measures might lead to positive effects in controlling the release of some heavy metals to the environment. However, environmental behaviors differed with geochemical characteristics of individual elements. Further remediation actions to reduce heavy metal pollution to the surrounding environment might still be needed.
  •  
7.
  • Fu, Jianjie, et al. (author)
  • Spatial distribution of polychlorinated biphenyls (PCBs) and polybrominated biphenyl ethers (PBDEs) in an e-waste dismantling region in Southeast China : use of apple snail (Ampullariidae) as a bioindicator
  • 2011
  • In: Chemosphere. - : Elsevier BV. - 0045-6535 .- 1879-1298. ; 82:5, s. 648-655
  • Journal article (peer-reviewed)abstract
    • Fengjiang is a large e-waste dismantling site located in southeast China. In this paper, apple snail and soil samples were collected from this e-waste dismantling site and 25 vicinal towns to investigate the contamination status, spatial distributions and congener patterns of polychlorinated biphenyls (PCBs) and polybrominated biphenyl ethers (PBDEs). Total PCB concentrations in apple snails (3.78-1812ngg(-1) dry weight (dw)) were significant higher than that in soil samples (0.48-90.1ngg(-1) dw). PBDE (excluding BDE 209) concentrations in apple snail and soil samples ranged from 0.09 to 27.7ngg(-1) dw and 0.06 to 31.2ngg(-1) dw, respectively. Concentrations of PCBs and PBDEs in snails and soils correlated negatively with the distance from Fengjiang. Both the concentrations and profiles of the pollutants were significantly correlated (p<0.05) between the snail and soil samples, indicating the suitability of apple snail as a reliable bioindicator for PCBs and PBDEs contamination in this region. Relatively high concentrations of PCBs and PBDEs at locations far from e-waste dismantling sites implied that these pollutants have been transported to surrounding regions.
  •  
8.
  • Fu, Jianjie, et al. (author)
  • Temporal trends (2005-2009) of PCDD/Fs, PCBs, PBDEs in rice hulls from an e-waste dismantling area after stricter environmental regulations
  • 2012
  • In: Chemosphere. - : Elsevier BV. - 0045-6535 .- 1879-1298. ; 88:3, s. 330-335
  • Journal article (peer-reviewed)abstract
    • Primitive e-waste dismantling activities have been of increasing concern due to serious environmental and human health problems, and therefore authorities in China have strengthened the regulations on illegal e-waste recycling activities. In this work, we used rice hull as a passive sampler and investigated temporal trends of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs) in areas near e-waste recycling sites after the stricter regulations. Furthermore, the distribution patterns and composition profiles of these contaminants were also discussed. The average concentrations of the three groups of persistent organic pollutants (POPs) in rice hulls have markedly decreased during the period of 2005-2009. Specifically, from 12.9 (average value in 2005) to 0.37 pg WHO-TEQ/g (dry weight, dw) (in 2009) for PCDD/Fs, 47.6 (2005) to 7.10 ng g(-1)dw (2009) for PCBs, and 2.51 (2005) to 0.89 ng g(-1), dw (2009) for PBDEs. The significant decrease of combustion markers 2,3,4,7,8-PeCDF, 1,2,3,6,7,8HxCDF and PCB126, and the PCDD/PCDF ratio from 1:9 (2005) to 7:3 (2009) is likely a result of stricter regulations on open combustion activities. This study suggests that stricter control measures, strengthened laws and regulations and more environmental friendly techniques could be effective measures in reducing the release and formation of related POPs in typical e-waste dismantling sites, and these measures could further improve the quality of the environment and health of the local inhabitants.
  •  
9.
  • Gao, Yan, et al. (author)
  • Differential accumulation and elimination behavior of perfluoroalkyl acid isomers in occupational workers in a manufactory in China
  • 2015
  • In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 49:11, s. 6953-6962
  • Journal article (peer-reviewed)abstract
    • In this study, serum and urine samples were collected from 36 occupational workers in a fluorochemical manufacturing plant in China from 2008 to 2012 to evaluate the body burden and possible elimination of linear and branched perfluoroalkyl acids (PFAAs). Indoor dust, total suspended particles (TSP), diet, and drinking water samples were also collected to trace the occupational exposure pathway to PFAA isomers. The geometric mean concentrations of perfluorooctanesulfonate (PFOS), perfluorooctanoate (PFOA), and perfluorohexanesulfonate (PFHxS) isomers in the serum were 1386, 371, and 863 ng mL(-1), respectively. The linear isomer of PFOS, PFOA, and PFHxS was the most predominant PFAA in the serum, with mean proportions of 63.3, 91.1, and 92.7% respectively, which were higher than the proportions in urine. The most important exposure routes to PFAA isomers in the occupational workers were considered to be the intake of indoor dust and TSP. A renal clearance estimation indicated that branched PFAA isomers had a higher renal clearance rate than did the corresponding linear isomers. Molecular docking modeling implied that linear PFOS (n-PFOS) had a stronger interaction with human serum albumin (HSA) than branched isomers did, which could decrease the proportion of n-PFOS in the blood of humans via the transport of HSA.
  •  
10.
  • Grasse, Patricia, et al. (author)
  • GEOTRACES inter-calibration of the stable silicon isotope composition of dissolved silicic acid in seawater
  • 2017
  • In: Journal of Analytical Atomic Spectrometry. - : Royal Society of Chemistry (RSC). - 0267-9477 .- 1364-5544. ; 32:3, s. 562-578
  • Journal article (peer-reviewed)abstract
    • The first inter-calibration study of the stable silicon isotope composition of dissolved silicic acid in seawater, delta Si-30(OH)(4), is presented as a contribution to the international GEOTRACES program. Eleven laboratories from seven countries analyzed two seawater samples from the North Pacific subtropical gyre (Station ALOHA) collected at 300 m and at 1000 m water depth. Sampling depths were chosen to obtain samples with a relatively low (9 mmol L-1, 300 m) and a relatively high (113 mmol L-1, 1000 m) silicic acid concentration as sample preparation differs for low- and highconcentration samples. Data for the 1000 m water sample were not normally distributed so the median is used to represent the central tendency for the two samples. Median delta Si-30(OH)(4) values of +1.66& for the low-concentration sample and +1.25& for the high-concentration sample were obtained. Agreement among laboratories is overall considered very good; however, small but statistically significant differences among the mean isotope values obtained by different laboratories were detected, likely reflecting inter-laboratory differences in chemical preparation including pre-concentration and purification methods together with different volumes of seawater analyzed, and the use of different mass spectrometers including the Neptune MC-ICP-MS (Thermo Fisher (TM), Germany), the Nu Plasma MC-ICP-MS (Nu Instruments (TM), Wrexham, UK), and the Finnigan (TM) (now Thermo Fisher (TM), Germany) MAT 252 IRMS. Future studies analyzing delta Si-30(OH)(4) in seawater should also analyze and report values for these same two reference waters in order to facilitate comparison of data generated among and within laboratories over time.
  •  
11.
  • GuangBo, Qu, et al. (author)
  • Detection of tris-(2,3-dibromopropyl) isocyanurate as a neuronal toxicant in environmental samples using neuronal toxicity-directed analysis
  • 2011
  • In: Science in China Series B. - : Science Press. - 1674-7291 .- 1869-1870. ; 54:10, s. 1651-1658
  • Journal article (peer-reviewed)abstract
    • Neuronal toxic pollutants in environment possess hazards to human health. It is essential to determine the causative neuronal toxicants in environmental samples. In the present study, viability of primary cultured cerebellar granule neurons (CGNs), combined with sample extraction, chemical fractionation and identification, was applied for screening acid-resistant neuronal toxic substances in environmental samples. River sediments and agricultural soils along the river near a brominated flame retardant (BFR) manufacturing plant in South China were collected to screen the key neuronal toxicants. The results indicated that the manufacturing plant was a source of neuronal toxicity risks. In the sediment and soil near the plant, one of the causative toxicants was identified as tris-(2,3-dibromopropyl) isocyanurate (TBC) using HPLC-MS/MS. In addition, an unknown chemical possibly causing significant neuronal toxicity was isolated from all the soil samples in the region.
  •  
12.
  •  
13.
  • Hao, Yanfen, et al. (author)
  • Air monitoring of polychlorinated biphenyls, polybrominated diphenyl ethers and organochlorine pesticides in West Antarctica during 2011-2017 : Concentrations, temporal trends and potential sources
  • 2019
  • In: Environmental Pollution. - : Elsevier. - 0269-7491 .- 1873-6424. ; 249, s. 381-389
  • Journal article (peer-reviewed)abstract
    • Annual air samples were collected at various sites in the Fildes Peninsula, West Antarctica from December 2010 to January 2018 using XAD-2 resin passive air samplers to investigate concentrations, temporal trends and potential sources of persistent organic pollutants (POPs) in Antarctic air. Relatively low concentrations of polychlorinated biphenyls (PCBs) (Σ19PCBs: 1.5-29.7 pg/m3), polybrominated diphenyl ethers (PBDEs) (Σ12PBDEs: 0.2-2.9 pg/m3) and organochlorine pesticides (OCPs) (Σ13OCPs: 101-278 pg/m3) were found in the atmosphere of West Antarctica. PCB-11, BDE-47 and hexachlorobenzene (HCB) were the predominant compounds in the atmosphere. The concentrations of PCBs, HCHs, DDTs and endosulfans were found to show decreasing temporal trends, whereas uniform temporal trends were observed for HCB. The atmospheric half-life values for PCBs, HCHs, DDTs and endosulfans in Antarctic air were estimated for the first time, using regressions of the natural logarithm of the concentrations versus the number of years, obtaining the values of 2.0, 2.0, 2.4 and 1.2 year, respectively. An increasing ratio of α-HCH/γ-HCH indicated long residence time for α-HCH and possible transformation of γ-HCH to α-HCH in the atmosphere. The ratios of p,p'-DDT/p,p'-DDE were mostly lower than unity in this study, which could be attributed to aged sources. It was found that long-range atmospheric transport was still considered to be the main contributing factor to the atmospheric levels of the POPs in West Antarctica whereas the contribution of human activities at the Chinese Great Wall Station was minor. The results of this study give a view on the most recent temporal trends and provide new insights regarding the occurrence of various POPs in the Antarctic atmosphere.
  •  
14.
  • Hu, Xialin, et al. (author)
  • DEVELOPMENT OF NEGLIGIBLE DEPLETION HOLLOW FIBER-PROTECTED LIQUID-PHASE MICROEXTRACTION FOR SENSING FREELY DISSOLVED TRIAZINES
  • 2009
  • In: Environmental Toxicology and Chemistry. - : Wiley. - 0730-7268 .- 1552-8618. ; 28:2, s. 231-238
  • Journal article (peer-reviewed)abstract
    • A new sampling method, termed negligible depletion hollow fiber-protected liquid-phase microextraction, was developed for sensing the freely dissolved concentration (C free) and evaluating the availability of atrazine (ATR), desethyl atrazine (DEA), and simazine (SIM) in water. The sampling device was prepared by impregnating 1-octanol to both the pores and the lumen of a piece of polypropylene microporous hollow fiber membrane. After equilibrium and negligible depletion extraction, the 1-octanol in the lumen of the hollow fiber (10 mu l) was collected for determination of triazines. Determination of C free and the distribution coefficient to 1-octanol (D-OW) can be performed with this technique. A wide linear working range (1-200 mu g/L) and low detection limits (0.1-1 mu g/L) were obtained for triazines. Measured log D-OW values of DEA (1.44 +/- 0.04), SIM (2.06 +/- 0.06), and ATR (2.33 +/- 0.05) agreed well with those reported in the literature. The measured D-OW values were independent of the chemical concentration and sample pH (pH 3-10) and negligibly affected by the sample salinity (0-500 mM), suggesting that environmentally relevant pH and salinity have no significant effects on the availability of triazines. Although a slight (<= 31%) increase of C free was observed, one-way analysis of variance indicated the C free of triazines were not significantly affected by the presence of Aldrich humic acid, Acros humic acid, and bovine albumin V (dissolved organic carbon [DOC], 0-100 mg/L). From 3 to 36% of the spiked triazines, however, were found to associate with the dissolved organic matter (DOM) in surface-water samples (DOC, 32.0-61.9 mg/L), suggesting the origin of the DOM is a key parameter in determining its association with and, thus, the availability of triazines.
  •  
15.
  • Li, Hongcheng, et al. (author)
  • Effects of waterborne nano-iron on medaka (Oryzias latipes) : antioxidant enzymatic activity, lipid peroxidation and histopathology
  • 2009
  • In: Ecotoxicology and Environmental Safety. - : Elsevier BV. - 0147-6513 .- 1090-2414. ; 72:3, s. 684-692
  • Journal article (peer-reviewed)abstract
    • Toxicity tests were performed to investigate possible harmful effects on medaka exposed to nano-iron. Dose-dependent decreases of superoxide dismutase (SOD) and increases of malondialdehyde (MDA) were induced in the medaka embryo, suggesting that oxidative damage was induced by nano-iron. For adult medaka, the disturbance of antioxidative balance was observed during the early exposure period based on the monitoring of the hepatic and cerebral SOD and reduced glutathione (GSH). No terminal oxidative damage occurred during the whole exposure period, probably due to the high self-recovering capability of the adult fish. Some histopathological and morphological alterations (cell swelling, hyperplasia, and granulomas, etc.) were observed in gill and intestine tissues, which confirmed that deleterious effects occurred as a result of direct contact with nano-iron. It is suggested that further evaluation should be made concerning the risk assessment of waterborne nano-iron on aquatic life.
  •  
16.
  • Li, Hongcheng, et al. (author)
  • Elemental selenium particles at nano-size (Nano-Se) are more toxic to Medaka (Oryzias latipes) as a consequence of hyper-accumulation of selenium : a comparison with sodium selenite
  • 2008
  • In: Aquatic Toxicology. - : Elsevier BV. - 0166-445X .- 1879-1514. ; 89:4, s. 251-256
  • Journal article (peer-reviewed)abstract
    • Recent studies have shown that elemental selenium particles at nano-size (Nano-Se) exhibited comparable bioavailability and less toxicity in mice and rats when compared to sodium selenite, selenomethinine and methylselenocysteine. However, little is known about the toxicity profile of Nano-Se in aquatic animals. In the present study, toxicities of Nano-Se and selenite in selenium-sufficient Medaka fish were compared. Selenium bioaccumulation and subsequent clearance in fish livers, gills, muscles and whole bodies were examined after 10 days of exposure to Nano-Se and selenite (100 microg Se/L) and again after 7 days of depuration. Both forms of selenium exposure effectively increased selenium concentrations in the investigated tissues. Surprisingly, Nano-Se was found to be more hyper-accumulated in the liver compared to selenite with differences as high as sixfold. Selenium clearance of both Nano-Se and selenite occurred at similar ratios in whole bodies and muscles but was not rapidly cleared from livers and gills. Nano-Se exhibited strong toxicity for Medaka with an approximately fivefold difference in terms of LC(50) compared to selenite. Nano-Se also caused larger effects on oxidative stress, most likely due to more hyper-accumulation of selenium in liver. The present study suggests that toxicity of nanoparticles can largely vary between different species and concludes that the evaluation of nanotoxicology should be carried out on a case-by-case basis.
  •  
17.
  • Li, Honghua, et al. (author)
  • Levels and distribution of hexabromocyclododecane (HBCD) in environmental samples near manufacturing facilities in Laizhou Bay area, East China
  • 2012
  • In: Journal of Environmental Monitoring. - : Royal Society of Chemistry (RSC). - 1464-0325 .- 1464-0333. ; 14:10, s. 2591-2597
  • Journal article (peer-reviewed)abstract
    • A total of 55 samples including soil, sediment, plants (cypress, reed and seepweed) and aquatic species were collected at locations around hexabromocyclododecane (HBCD) manufacturing facilities in Laizhou Bay area, East China. HBCD was determined at concentrations ranging between 0.88 and 6901 ng g(-1) dry weight (dw), 2.93-1029 ng g(-1) dw, 8.88-160241 ng g(-1) dw, and 7.09-815 ng g(-1) lipid weight (lw), respectively. Significant negative correlations (r(2) = 0.54, p = 0.006) were observed between HBCD concentrations in soils and the distance from the manufacturing facility, and the concentrations became constant when the distance was >4 km. The calculation results on the bioaccumulation factors (BAFs) suggested that HBCD may be accumulated in plants. Tissue-specific bioaccumulation of HBCD diastereoisomers was found in aquatic species. For example, in crabs the highest concentrations of HBCD (815 ng g(-1) lw for female and 446 ng g(-1) lw for male) were observed in the gill. Besides the gill, α-HBCD was more preferentially accumulated in the spermary and ovary, while β- and γ-HBCD were more accumulated in the muscle. A similar distribution was also observed in roe and muscle of goby fish.
  •  
18.
  • Li, Yingming, et al. (author)
  • Atmospheric distribution of polychlorinated dibenzo-p-dioxins, dibenzofurans and dioxin-like polychlorinated biphenyls around a steel plant area, northeast China
  • 2010
  • In: Chemosphere. - : Elsevier BV. - 0045-6535 .- 1879-1298. ; 79:3, s. 253-258
  • Journal article (peer-reviewed)abstract
    • Air monitoring of polychlorinated dibenzo-p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs), and dioxin-like polychlorinated biphenyls (PCBs) was carried out in June 2008 and January 2009 to investigate the concentrations, profiles and estimating potential inhalation risks to the local residents around a steel plant area in northeast China. The air concentrations and WHO-TEQs of PCDD/Fs ranged 94-4944fgm(-3) (average 1352fgm(-3)) and 3-247fgm(-3) (average 81fgm(-3)), respectively. The WHO-TEQ concentrations of dioxin-like PCBs ranged 1-18fgm(-3) (average 5fgm(-3)), contributing to 3.6-26% of the total TEQ. Higher PCDD/F concentrations were observed in the winter, whereas higher dioxin-like PCB concentrations were found in the summer. The seasonal trend can be related to the significant correlation between the concentrations of dioxins and the reciprocal of temperature (positive for PCDD/Fs, P<0.01; negative for dioxin-like PCBs, P=0.05). A significant positive correlation (P<0.0001) was found between the concentration of total suspended particulate (TSP) and PCDD/F concentrations, but not for PCB congeners. Although the steel plant sites showed higher dioxin levels than the residential and background areas, the PCDD/F levels in the atmosphere of the steel plant area was at a relatively low level. The results from this study provides further aid in evaluating the impact of steel plants as PCDD/Fs emission sources to the ambient air in China.
  •  
19.
  • Li, YingMing, et al. (author)
  • Levels and distribution of polychlorinated biphenyls in the atmosphere close to Chinese Great Wall Station, Antarctica : Results from XAD-resin passive air sampling
  • 2012
  • In: Chinese Science Bulletin. - Beijing : Science Press. - 1001-6538 .- 1861-9541. ; 57:13, s. 1499-1503
  • Journal article (peer-reviewed)abstract
    • Antarctica is an important research region for assessing persistence and long-range atmospheric transport (LRAT) of persistent organic pollutants (POPs). In this study, XAD-resin passive air sampling was conducted near the Chinese Great Wall Station, Antarctica, during a one-year sampling period in 2009-2010. The air concentrations of polychlorinated biphenyls (PCBs) were at a very low level, with total PCBs in the range of 26.74-45.08 pg m(-3). PCB profiles were dominated by tetra-PCBs, tri-PCBs and di-PCBs, indicating LRAT was responsible for the pollutants in the Antarctic atmosphere. The sampling site near the Chinese Great Wall Station did not show higher PCB levels than the other sites, suggesting that PCB sources associated with the Great Wall Station were negligible. PCB-11 is a non-Aroclor congener, which has specific sources compared to other Aroclor PCB congeners. PCB-11 was observed in all air samples, with an average concentration of 1.22 pg m(-3). To our knowledge, this study is the first investigation of PCB levels and distribution in the atmosphere around the Chinese Great Wall Station, Antarctica.
  •  
20.
  • Li, Yingming, et al. (author)
  • Levels and vertical distributions of PCBs, PBDEs, and OCPs in the atmospheric boundary layer : observation from the Beijing 325-m meteorological tower
  • 2009
  • In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 43:4, s. 1030-1035
  • Journal article (peer-reviewed)abstract
    • Polyurethane foam disk passive air sampling was carried out to investigate the levels, vertical distributions, and potential sources of polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs) and organochlorine pesticides (OCPs) in the atmospheric boundary layer of an urban site in Asia. Sampling was performed at nine heights (15, 47, 80, 120, 160, 200, 240, 280, 320 m) of the 325-m meteorological tower in Beijing, China over three 2-month periods between December 2006 and August 2007. This is the first study to report vertical variations of PBDEs in the ABL and one of only a few studies to investigate vertical distributions of persistent organic pollutants. The levels of sigma19PCBs and sigma8PBDEs were relatively low, ranging from 22 to 65 and from 2.3 to 18 pg m-3, respectively. Air concentrations of gamma-HCH were high, with values in the range of 39-103 pg m-3 in winter, 100-180 pg m-3 in spring, and 115-242 pg m-3 in summer, respectively. alpha-HCH concentrations ranged from 20 to 86 pg m-3, p,p'-DDT between 7.3 and 78 pg m-3, and HCB between 15 and 160 pg m-3. The seasonal variations of PCBs, PBDEs, and OCPs may reflect different sources for these chemicals, such as those related with regional use (gamma-HCH), volatilization/re-emission (PBDEs, PCBs, alpha-HCH), and pesticide impurities (HCB). Although the performance reference compounds (PRCs) were spiked before deployment, the sampling rates showed strong dependency on wind speeds, resulting in large variations in uptake rates in the ABL, ranging from approximately 7.0 m3 day-1 at ground level to 11 m3 day-1 at 320 m. Levels of PCBs, PBDEs, and OCPs decreased with increasing ABL height indicating the potential of Beijing as the local sources.
  •  
21.
  • Li, Yongting, et al. (author)
  • Organophosphate Flame Retardants in Pregnant Women : Sources, Occurrence, and Potential Risks to Pregnancy Outcomes
  • 2023
  • In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 57:18, s. 7109-7128
  • Research review (peer-reviewed)abstract
    • Organophosphate flame retardants (OPFRs) are found in various environmental matrixes and human samples. Exposure to OPFRs during gestation may interfere with pregnancy, for example, inducing maternal oxidative stress and maternal hypertension during pregnancy, interfering maternal and fetal thyroid hormone secretion and fetal neurodevelopment, and causing fetal metabolic abnormalities. However, the consequences of OPFR exposure on pregnant women, impact on mother-to-child transmission of OPFRs, and harmful effects on fetal and pregnancy outcomes have not been evaluated. This review describes the exposure to OPFRs in pregnant women worldwide, based on metabolites of OPFRs (mOPs) in urine for prenatal exposure and OPFRs in breast milk for postnatal exposure. Predictors of maternal exposure to OPFRs and variability of mOPs in urine have been discussed. Mother-to-child transmission pathways of OPFRs have been scrutinized, considering the levels of OPFRs and their metabolites in amniotic fluid, placenta, deciduae, chorionic villi, and cord blood. The results showed that bis(1,3-dichloro-2-propyl) phosphate (BDCIPP) and diphenyl phosphate (DPHP) were the two predominant mOPs in urine, with detection frequencies of >90%. The estimated daily intake (EDIM) indicates low risk when infants are exposed to OPFRs from breast milk. Furthermore, higher exposure levels of OPFRs in pregnant women may increase the risk of adverse pregnancy outcomes and influence the developmental behavior of infants. This review summarizes the knowledge gaps of OPFRs in pregnant women and highlights the crucial steps for assessing health risks in susceptible populations, such as pregnant women and fetuses.
  •  
22.
  • Li, Yingming, et al. (author)
  • Reduction of atmospheric polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) during the 2008 Beijing Olympic games
  • 2011
  • In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 45:8, s. 3304-3309
  • Journal article (peer-reviewed)abstract
    • A total of 120 air samples were collected at three urban and one rural location in Beijing, China in the summers of 2007-2010, and before, during, and after the Beijing 2008 Olympic Games (BOG), in order to assess the effectiveness of long-term and short-term emission-control measures in reducing polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in the atmosphere. During the BOG (August, 2008), the PCDD/Fs concentrations decreased to an average value of 1150 fg m−3 (63 fg I-TEQ m−3), which was reduced by approximately 70% from the average in 2007 and by 29% from that in July 2008, before the Olympic event began. Although 2009-2010 levels of PCDD/Fs were significantly higher than 2008, the overall temporal trend was decreasing for summer months during the sampling campaign period. The apparent half-lives of atmospheric PCDD/Fs were estimated to be 3.2-5.8 years by statistically regressing the logarithm PCDD/Fs concentrations versus the number of years passed since 2006. The air concentrations of total suspended particulates (TSP) during the BOG ranged between 135 and 183 μg m−3, showing a 52% reduction from 2007 and 26% decrease from those prior to the Olympic event. No significant relationships were found between meteorological parameters (temperature, humidity, and wind speed) and PCDD/Fs or TSP during the BOG, whereas the PCDD/Fs concentrations were significantly dependent on the air quality (p < 0.05, positive against TSP and negative against visibility). This work is one of few temporal trend studies of atmospheric PCDD/Fs in mainland China, and provides unique insight into the effects of large-scale control measures in improving air quality and reducing one of the most ubiquitous and toxic organic pollutants in the environment.
  •  
23.
  • Li, Yingming, et al. (author)
  • Study of PCBs and PBDEs in King George Island, Antarctica, using PUF passive air sampling
  • 2012
  • In: Atmospheric Environment. - : Elsevier. - 1352-2310 .- 1873-2844. ; 51, s. 140-145
  • Journal article (peer-reviewed)abstract
    • Polyurethane foam (PUF)-disk based passive air samplers were deployed in King George Island, Antarctica, during the austral summer of 2009-2010, to investigate levels, distributions and potential sources of polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) in Antarctic air. The atmospheric levels of Sigma indicator PCBs and Sigma(14) PBDEs ranged from 1.66 to 6.50 pg m(-3) and from 0.67 to 2.98 pg m(-3), respectively. PCBs homologue profiles were dominated by di-PCBs, tri-PCBs and tetra-PCBs, whereas BDE-17 and BDE-28 were the predominant congeners of PBDEs, which could be explained by long-range atmospheric transport processes. However, the sampling sites close to the Antarctic research stations showed higher atmospheric concentrations of PCBs and PBDEs than the other sites, reflecting potential local sources from the Antarctic research stations. The non-Aroclor congener PCB-11 was found in all the air samples, with air concentrations of 3.60-31.4 pg m(-3) (average 15.2 pg m(-3)). Comparison between the results derived from PUF-disk passive air sampling and high-volume air sampling validates the feasibility of using the passive air samplers in Antarctic air. To our knowledge, this study is the first employment of PUF-disk based passive air samplers in Antarctic atmosphere.
  •  
24.
  • Li, Zhuona, et al. (author)
  • Effects of polycyclic musks HHCB and AHTN on steroidogenesis in H295R cells
  • 2013
  • In: Chemosphere. - : Elsevier. - 0045-6535 .- 1879-1298. ; 90:3, s. 1227-1235
  • Journal article (peer-reviewed)abstract
    • 1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta-(γ)-2-benzopyran (HHCB) and 7-acetyl-1,1,3,4,4,6-hexamethyl-1,2,3,4-tetrahydronaphthalene (AHTN) are widely used in personal care products. Previous studies showed that HHCB and AHTN can be found in various environmental matrices and have potential endocrine disrupting effects. However, the effects on adrenocortical function of HHCB and AHTN are not fully understood. This study evaluated the influences of HHCB and AHTN on seven steroid hormones (progesterone, aldosterone, cortisol, 17α-OH-progesterone, androstenedione, 17β-estradiol, and testosterone) and 10 genes involved in steroidogenic pathways (HMGR, StAR, CYP11A1, 3βHSD2, CYP17, CYP21, CYP11B1, CYP11B2, 17βHSD, and CYP19) using the H295R cell line in the absence and presence of 8-Br-cAMP. MC2R transcription on the cell membrane was also examined to further investigate the effects of HHCB and AHTN on adrenal steroidogenesis. The results demonstrated that HHCB and AHTN could inhibit progesterone and cortisol production mainly by the suppression of 3βHSD2 and CYP21. Meanwhile, high concentrations of AHTN can affect the sensitivity of H295R cells to ACTH by disrupting MC2R transcription. Overall, the results indicate that high concentrations of HHCB and AHTN can affect steroidogenesis in vitro using the H295R cell line.
  •  
25.
  • Liao, Chunyang, et al. (author)
  • Changes in synaptic transmission, calcium current, and neurite growth by perfluorinated compounds are dependent on the chain length and functional group
  • 2009
  • In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 43:6, s. 2099-2104
  • Journal article (peer-reviewed)abstract
    • Scientific and public concerns on perfluorinated compounds (PFCs) are increasingly growing because of their environmental persistency, bioaccumulation, and extensive distribution throughout the world. Little is known about the effects of PFCs on neural function and the underlying mechanisms. Recent evidence suggests that the toxicological effects of PFCs are closely correlated with their carbon chain lengths. In this present work, the actions of PFCs with varying chain length on cultured rat hippocampal neurons and possible action patterns were examined. Increases in the frequencies of spontaneous miniature postsynaptic current (mPSC) were commonly found in cultured neurons when perfused with PFCs. The increase of mPSC frequency was in proportion to the carbon chain length, and the potency of perfluorinated carboxylates was less pronounced than that of perfluorinated sulfonates. A comparable but less perceptible trend was also found for the amplitudes of voltage-dependent calcium current (ICa). No regular change in pattern was observed for the effects of PFCs on activation and inactivation kinetics of ICa. Furthermore, prolonged treatment of PFCs inhibited the neurite growth of neuronsto various degrees. Comparisons between nonfluorinated and perfluorinated analogues demonstrated thatthefluorination in alkyl chain exerts stronger actions on neurons as compared to the surfactant activity. This study shows that PFCs exhibit adverse effects on cultured neurons to various extents, which is dependent on the carbon chain length and functional group attached to the fully fluorinated alkyl chain.
  •  
26.
  • Liu, Qian, et al. (author)
  • Evaluation of graphene as an advantageous adsorbent for solid-phase extraction with chlorophenols as model analytes
  • 2011
  • In: Journal of Chromatography A. - : Elsevier. - 0021-9673 .- 1873-3778. ; 1218:2, s. 197-204
  • Journal article (peer-reviewed)abstract
    • Graphene, a novel class of carbon nanostructures, possesses an ultrahigh specific surface area, and thus has great potentials for the use as sorbent materials. We herein demonstrate the use of graphene as a novel adsorbent for solid-phase extraction (SPE). Eight chlorophenols (CPs) as model analytes were extracted on a graphene-packed SPE cartridge, and then eluted with alkaline methanol. The concentrations in the eluate were determined by HPLC with multi-wavelength UV detection. Under the optimized conditions, high sensitivity (detection limits 0.1-0.4 ng/mL) and good reproducibility of CPs (RSDs 2.2-7.7% for run-to-run assays) were achieved. Comparative studies showed that graphene was superior to other adsorbents including C18 silica, graphitic carbon, single- and multi-walled carbon nanotubes for the extraction of CPs. Some other advantages of graphene as SPE adsorbent, such as good compatibility with various organic solvents, good reusability and no impact of sorbent drying, have also been demonstrated. The proposed method was successfully applied to the analysis of tap and river water samples with recoveries ranging from 77.2 to 116.6%. This work not only proposes a useful method for environmental water sample pretreatment, but also reveals great potentials of graphene as an excellent sorbent material in analytical processes.
  •  
27.
  •  
28.
  • Liu, Qian, et al. (author)
  • Graphene-assisted matrix solid-phase dispersion for extraction of polybrominated diphenyl ethers and their methoxylated and hydroxylated analogs from environmental samples
  • 2011
  • In: Analytica Chimica Acta. - : Elsevier. - 0003-2670 .- 1873-4324. ; 708:1-2, s. 61-68
  • Journal article (peer-reviewed)abstract
    • In this work, we developed a novel graphene-assisted matrix solid-phase dispersion (GA-MSPD) method for extraction of polybrominated diphenyl ethers (PBDEs) and their methoxylated (MeO-) and hydroxylated (OH-) analogs from environmental samples. We found that grinding the solid sample with chemically converted graphene (CCG) powder yielded a tight contact and sufficient dispersion of the sample matrix due to the large surface area and flexible nanosheet morphology of CCG. The resultant blend was eluted using a two-step elution strategy: PBDEs and MeO-PBDEs were eluted firstly by hexane/dichloromethane and analyzed by GC-ECD, and then OH-PBDEs were eluted by acetone and determined by LC-ESI-MS/MS. The GA-MSPD conditions were optimized in detail. Better recoveries were obtained with GA-MSPD than with other sorbents (C18 silica, Florisil and carbon nanotubes) and other extraction techniques (Soxhlet and accelerated solvent extraction). Other advantages of GA-MSPD, including reduced consumption of sorbent and solvent, good selectivity and short extraction time, were also demonstrated. In analysis of soil samples, the method detection limits of five PBDEs, ten MeO-PBDEs and ten OH-PBDEs were in the range of 5.9-28.7, 14.3-46.6, and 5.3-212.6 pg g(-1) dry weight, respectively. The proposed method was successfully applied to the extraction of PBDEs, MeO-PBDEs and OH-PBDEs from different kinds of spiked environmental samples, including soil, tree bark and fish.
  •  
29.
  • Liu, Qian, et al. (author)
  • Graphenized pencil lead fiber : facile preparation and application in solid-phase microextraction
  • 2014
  • In: Journal of Chromatography A. - : Elsevier. - 0021-9673 .- 1873-3778. ; 1325, s. 1-7
  • Journal article (peer-reviewed)abstract
    • Graphenized pencil lead fiber was facilely prepared by in situ chemical exfoliation of graphite in pencil lead fiber to few-layered graphene sheets via a one-pot, one-step pressurized oxidation reaction for the first time. This new fiber was characterized and demonstrated to be a highly efficient but low-cost solid-phase microextraction (SPME) fiber. The extraction performance of the fiber was evaluated with four bisphenol analogs [bisphenol A (BPA), bisphenol S (BPS), bisphenol AF (BPAF), and tetrabromobisphenol A (TBBPA)] as model analytes in direct SPME mode. Unlike commercially available fibers, the graphenized pencil lead fiber showed an excellent chemical stability in highly saline, acidic, alkaline and organic conditions due to its coating-free configuration. The fiber also showed a very long lifespan. Furthermore, high extraction efficiency and good selectivity for the analytes with a wide polarity range could be obtained due to the exceptional properties of graphene. The detection limits (LODs) for the analytes were in the range of 1.1-25ng/L. The fiber was successfully applied in the analysis of tap water and effluent samples from a waste water treatment plant with spike recoveries ranging from 68.5 to 105.1%. Therefore, the graphenized pencil lead fiber provides a high performance, cheap, robust, and reliable tool for SPME.
  •  
30.
  • Liu, Qian, et al. (author)
  • Hemimicelles/admicelles supported on magnetic graphene sheets for enhanced magnetic solid-phase extraction
  • 2012
  • In: Journal of Chromatography A. - : Elsevier. - 0021-9673 .- 1873-3778. ; 1257, s. 1-8
  • Journal article (peer-reviewed)abstract
    • In this work, superparamagnetic nanoparticle-decorated graphene (MG) sheets were synthesized and used as support for hemimicelles/admicelles for solid-phase extraction (SPE) of different compounds from environmental water samples for the first time. The MG sheets were facilely synthesized by a one-step, one-pot redox reaction between graphene oxide and Fe(II). Due to the large surface area and unique nanosheet morphology, MG served as an excellent nano-scaled support material for hemimicelles and admicelles, exhibiting higher loading capacity than conventional materials and pure Fe₃O₄ nanoparticles. The MG sheets could be negatively or positively charged depending on solution pH, allowing the extraction to be conducted in different modes. In cationic mode, cetyltrimethylammonium bromide (CTAB) was used as micelle-forming reagent, and perfluoroalkyl and polyfluoroalkyl substances (PFASs) and alkylphenols were used as model analytes. In anionic mode, sodium dodecyl sulfate (SDS) was used as micelle-forming reagent and alkyltrimethylammonium salts were selected as analytes. In both modes, the formation processes of hemimicelles/admicelles on MG sheets were studied and the extraction conditions were optimized. For PFASs, the analytical sensitivity was enhanced by 50-113-fold by the extraction, and the method detection limits (MDLs) ranged from 0.15 to 0.50 ng/L. For alkyltrimethylammonium salts, the MDLs were in the range of 1.4-8.0 ng/L. In both modes, good recoveries (56.3-93.9%) and reproducibility (run-to-run RSDs<9.3%) were obtained. The results from this work show a potential new role of graphene in analytical sample preparation.
  •  
31.
  • Liu, Runzeng, et al. (author)
  • Determination of nine benzotriazole UV stabilizers in environmental water samples by automated on-line solid phase extraction coupled with high-performance liquid chromatography-tandem mass spectrometry
  • 2014
  • In: Talanta. - : Elsevier. - 0039-9140 .- 1873-3573. ; 120, s. 158-166
  • Journal article (peer-reviewed)abstract
    • A method using automated on-line solid phase extraction coupled with a high-performance liquid chromatography-tandem mass spectrometry system was developed for the determination of emerging benzotriazole UV stabilizers (BZTs) in different environmental water matrices including river water, sewage influent and effluent. Water sample was injected directly and the analytes were preconcentrated on a Polar Advantage II on-line SPE cartridge. After cleanup step the target BZTs were eluted in back flush mode and then separated on a liquid chromatography column. Experimental parameters such as sample loading flow rate, SPE cartridge, pH value and methanol ratio in the sample were optimized in detail. The method detection limits ranged from 0.21 to 2.17 ng/L. Recoveries of the target BZTs at 50 ng/L spiking level ranged from 76% to 114% and the inter-day RSDs ranged from 1% to 15%. The optimized method was successfully applied to analyze twelve water samples collected from different wastewater treatment plants and rivers, and five BZTs (UV-P, UV-329, UV-350, UV-234 and UV-328) were detected with concentrations up to 37.1 ng/L. The proposed method is simple, sensitive and suitable for simultaneous analysis and monitoring of BZTs in water samples.
  •  
32.
  • Liu, Runzeng, et al. (author)
  • Trace analysis of mono-, di-, tri-substituted polyfluoroalkyl phosphates and perfluorinated phosphonic acids in sewage sludge by high performance liquid chromatography tandem mass spectrometry
  • 2013
  • In: Talanta. - : Elsevier. - 0039-9140 .- 1873-3573. ; 111, s. 170-177
  • Journal article (peer-reviewed)abstract
    • A new method using ultrasonic extraction and solid phase extraction (SPE) clean-up pretreatments was developed for the analysis of mono-, di- and tri-substituted polyfluoroalkyl phosphates (abbreviated as mono-PAPs, di-PAPs and tri-PAPs) and perfluorinated phosphonic acids (PFPAs) in sludge from wastewater treatment plants (WWTPs). For the ultrasonic extraction of three mono-PAPs, three di-PAPs and three PFPAs in sludge samples, a mixture of tetrahydrofuran/acetic acid (1:1, v/v) was found to be the most suitable extraction solvent. The subsequently optimized clean-up and enrichment procedures were carried out with weak anion exchange (WAX) cartridges in-line coupled with graphitized carbon black (ENVI-Carb) tubes. Two tri-PAPs were ultrasonically extracted by acetonitrile/tetrahydrofuran (1:1, v/v) and cleaned by mixed-mode anion exchange (MAX) in-line coupled with ENVI-Carb cartridges. The analytes were analyzed by optimized high performance liquid chromatography tandem mass spectrometry (HPLC-MS/MS) method either in negative or positive ionization mode. The method quantification limits (MQLs) of the 11 analytes in sludge ranged from 0.6 to 5.1 ng/g, meanwhile the total recoveries of the pretreatment varied from 24% (6:2 mono-PAP) to 107% (PFDPA). The method was successfully applied to analyze 16 sewage sludge samples collected from seven provinces in China, and two mono-PAPs were identified with concentrations ranging from
  •  
33.
  • Liu, Yanna, et al. (author)
  • High-resolution mass spectrometry (HRMS) methods for nontarget discovery and characterization of poly- and per-fluoroalkyl substances (PFASs) in environmental and human samples
  • 2019
  • In: TrAC. Trends in analytical chemistry. - : Elsevier BV. - 0165-9936 .- 1879-3142. ; 121
  • Research review (peer-reviewed)abstract
    • Widespread environmental contamination of legacy long-chain poly- and per-fluoroalkyl substances (PFASs) has triggered chemical regulatory action and a global transitioning to alternative PFASs. More than 5000 PFASs are now recognized on various lists, but few have been monitored despite ample evidence of unidentified organic fluorine in human and environmental samples. Nevertheless, our review of the literature indicates that nontarget analytical methods based on high-resolution mass spectrometry have been used to discover more than 750 PFASs, belonging to more than 130 diverse classes, in strategically selected environmental samples, biofluids or commercial products. Among these reports, we summarize the analytical and data-processing strategies for nontarget PFAS discovery, identify knowledge gaps and propose new areas for method development. Discovery of emerging PFASs before they are global contaminants could mitigate future contamination if strategic techniques can be developed to prioritize some of these substances for synthesis and confirmation, further monitoring, source elucidation and hazard characterization. 
  •  
34.
  • Qu, Guangbo, et al. (author)
  • Identification of tetrabromobisphenol A allyl ether and tetrabromobisphenol A 2,3-dibromopropyl ether in the ambient environment near a manufacturing site and in mollusks at a coastal region
  • 2013
  • In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 47:9, s. 4760-4767
  • Journal article (peer-reviewed)abstract
    • Tetrabromobisphenol A (TBBPA) is one of the most widely used brominated flame retardants (BFRs) and has been frequently detected in the environment and biota. Recent studies have found that derivatives of TBBPA, such as TBBPA bis(allyl) ether (TBBPA BAE) and TBBPA bis(2,3-dibromopropyl) ether (TBBPA BDBPE) are present in various environmental compartments. In this work, using liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) and liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (LC-Q-TOF-MS), TBBPA allyl ether (TBBPA AE) and TBBPA 2,3-dibromopropyl ether (TBBPA DBPE) were identified in environmental samples and further confirmed by synthesized standards. Soil, sediment, rice hull, and earthworm samples collected near a BFR manufacturing plant were found to contain these two compounds. In sediments, the concentrations of TBBPA AE and TBBPA DBPE ranged from 1.0 to 346.6 ng/g of dry weight (dw) and from 0.7 to 292.7 ng/g of dw, respectively. TBBPA AE and TBBPA DBPE in earthworm and rice hull samples were similar to soil samples, which ranged from below the method limit of detection (LOD, <0.002 ng/g of dw) to 0.064 ng/g of dw and from below the LOD (<0.008 ng/g of dw) to 0.58 ng/g of dw, respectively. Furthermore, mollusks collected from the Chinese Bohai Sea were used as a bioindicator to investigate the occurrence and distribution of these compounds in the coastal environment. The detection frequencies of TBBPA AE and TBBPA DBPE were 41 and 32%, respectively, and the concentrations ranged from below LOD (<0.003 ng/g of dw) to 0.54 ng/g of dw, with an average of 0.09 ng/g of dw, for TBBPA AE, and from below LOD (<0.008 ng/g of dw) to 1.41 ng/g of dw, with an average of 0.15 ng/g of dw, for TBBPA DBPE.
  •  
35.
  • Qu, Guangbo, et al. (author)
  • Identification of tetrabromobisphenol A diallyl ether as an emerging neurotoxicant in environmental samples by bioassay-directed fractionation and HPLC-APCI-MS/MS
  • 2011
  • In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 45:11, s. 5009-5016
  • Journal article (peer-reviewed)abstract
    • Brominated flame retardants (BFRs) have been widely used as additives in products to reduce their flammability. Recent findings suggested that some BFRs exhibit neurotoxicity and thus might pose a threat to human health. In this work, a neurotoxicity assay-directed analysis was developed, combining sample cleanup, fractionation, chemical identification, and bioassay. Viability of primary cultured cerebellar granule neurons (CGNs) was used to evaluate the neurotoxicity of extracts or separated fractions from environmental samples. Tetrabromobisphenol A diallyl ether (TBBPA DAE) was identified as the causative toxicant in sediment samples collected from a river near a brominated flame retardant (BFR) manufacturing plant in South China. Liquid chromatography atmospheric pressure chemical ionization tandem mass spectrometry (LC-APCI-MS/MS) was optimized to determine TBBPA DAE levels in the potent fractions and to confirm TBBPA DAE as the key neurotoxicant. On the basis of comparison with the structure of other TBBPA derivatives, the 1-propenyl group in TBBPA DAE appears to be the cause for the neurotoxic potency. The levels of TBBPA DAE in samples along the river were found at up to 49 ng/L for river water, 10,183 ng/g dry weight (dw) in surface sediments, and 42 ng/g dw in soils. According to the distribution of TBBPA DAE in the environmental samples, the manufacturing plant was identified as the release source of TBBPA DAE. To our knowledge, this study is the first to demonstrate potential neurotoxicity induced by TBBPA DAE in real environmental samples.
  •  
36.
  • Ruan, Ting, et al. (author)
  • Concentrations and composition profiles of benzotriazole UV stabilizers in municipal sewage sludge in China
  • 2012
  • In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 46:4, s. 2071-2079
  • Journal article (peer-reviewed)abstract
    • The environmental contamination and fate of benzotriazole UV stabilizers (BZTs) have received increasing attention due to their large production volume and wide usage in various consumer and industrial products. In the present work, 60 municipal sewage sludge samples from wastewater treatment plants (WWTPs) in 33 cities in China were collected to investigate the occurrence and distribution of 9 frequently used BZTs. The most dominant analogue was 2-[3,5-bis(1-methyl-1-phenylethyl)-2-hydroxyphenyl]benzotriazole (UV-234) at a median concentration of 116 ng/g (dry weight) and accounted on average for 27.2% of total BZTs. The abundance was successively followed by 2-(2-hydroxy-5-tert-octylphenyl)benzotriazole (UV-329, average 24.3%), 2-(2-hydroxy-3-tert-butyl-5-methylphenyl)-5-chlorobenzotriazole (UV-326, average 22.2%), 2-(3,5-di-tert-amyl-2-hydroxyphenyl)benzotriazole (UV-328, average 17.7%), and 2-(2-hydroxy-5-methylphenyl)benzotriazole (UV-P, average 6.6%), with median concentrations of 66.8, 67.8, 57.3, and 20.6 ng/g, respectively. 5-Chloro-2-(3,5-di-tert-butyl-2-hydroxyphenyl)benzotriazole (UV-327) and 2-(3-sec-butyl-5-tert-butyl-2-hydroxyphenyl)benzotriazole (UV-350) had low detection frequency, while 2-(3,5-di-tert-butyl-2-hydroxyphenyl)benzotriazole (UV-320) and 2-(5-tert-butyl-2-hydroxyphenyl)benzotriazole (UV-PS) were not detectable in any sample. To our knowledge, this is the first study reporting the occurrence of UV-234, UV-329, and UV-350 in sewage sludge in China. Significant correlations were found among the BZT concentrations and also with a WWTP characteristic (daily treatment volume). Furthermore, results from degradation prediction and multimedia fate simulation based on a quantitative structure-property relationship (QSPR) model at screening level also implied that the commercial BZT chemicals and their plausible transformation products might be persistent in the environment.
  •  
37.
  •  
38.
  • Ruan, Ting, et al. (author)
  • Identification and composition of emerging quaternary ammonium compounds in municipal sewage sludge in China
  • 2014
  • In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 48:8, s. 4289-4297
  • Journal article (peer-reviewed)abstract
    • Quaternary ammonium compounds (QACs) have raised considerable attention due to their wide commercial applications and recent discovery of unknown persistent analogues in aqueous environment. In this work, the occurrence and distribution of alkyltrimethylammonium (ATMAC), benzylakyldimethylethylammonium (BAC) and dialkyldimethylammonium (DADMAC) homologues were investigated in fifty-two municipal sewage sludge samples. ATMAC C10-18, BAC C8-18 and paired DADMAC C8:8-C18:18 as well as emerging homologues such as ATMAC-20, 22 and mixed DADMAC-16:18 and 14:16 were present. Furthermore, paired DADMAC-20:20 and mixed DADMAC-14:18, 18:20 were identified for the first time by nontarget qualitative strategies. A triple quadruple mass spectrometer quantification method was also initially verified with the aid of laboratory synthesized standards for the analysis of the mixed DADMACs with no certificated commercial standards currently available. The total concentrations of ATMACs, BACs and DADMACs were in the range of 0.38-293, 0.09-191 and 0.64-344 μg/g dry weight, respectively, and particularly, mixed DADMACs constituted 39 ± 7% of total DADMAC concentrations. The concentrations and profiles of individual homologues further suggested different QAC applications and fate in China. Significant correlations were also found among the concentrations of various QAC homologues as well as wastewater treatment plant (WWTP) characteristics (total organic carbon contents and daily treatment volumes).
  •  
39.
  • Ruan, Ting, et al. (author)
  • Identification and evaluation of a novel heterocyclic brominated flame retardant tris(2,3-dibromopropyl) isocyanurate in environmental matrices near a manufacturing plant in southern China
  • 2009
  • In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 43:9, s. 3080-3086
  • Journal article (peer-reviewed)abstract
    • A brominated flame retardant (BFR), hexabrominated heterocyclic tris-(2,3-dibromopropyl) isocyanurate (TBC), was identified,forthe first time, in the natural environment.The chemical was found in river water (2.33-163 ng/L), surface sediments (85.0 ng/g-6.03 microg/g dry weight (dw)), soils (19.6-672 ng/g dw), earthworm (9.75-78.8 ng/g dw), and carp samples (12.0-646 ng/g dw) from a factory-polluted area in southern China. It was found that TBC can strongly adsorb to organic material in sediment, and a trend of decreasing concentration with distance from the source in soil and earthworm samples, combined with calculated Kow (octanol-water partition coefficient) and Koa (octanol-air partition coefficient), suggests its potential ability to undergo regional transportation through dust deposition. Calculated results showed high Kow (log Kow = 7.37) and bioaccumulation factor (BAF) (log BAF = 4.30) of this BFR and indicate that TBC has semivolatile properties and bioaccumulation characteristic in certain biological species. Quantitative structure property relationships (QSPRs) modeling revealed that TBC has Koa (log Koa = 23.68) and Kaw (air-water partition coefficient) (log Kaw = -16.31) values several orders higher than those of other BFRs. The identification of this chemical additive further reminds us that the production and usage of heterocyclic BFRs may cause potential contamination to the surrounding environment
  •  
40.
  • Ruan, Ting, et al. (author)
  • Identification of novel polyfluorinated ether sulfonates as PFOS alternatives in municipal sewage sludge in China
  • 2015
  • In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 49:11, s. 6519-6527
  • Journal article (peer-reviewed)abstract
    • A 6:2 chlorinated polyfluorinated ether sulfonate (6:2 Cl-PFAES) with the trade name F-53B, is an alternative to perfluorooctanesulfonate (PFOS) in electroplating industry that is uniquely used in China. It was developed as a mist suppressant initially in the 1970s, but the environmental behaviors and potential adverse effects of the 6:2 Cl-PFAES have only recently been investigated. In this work, the occurrence and distribution of perfluoroalkyl sulfonate (PFSA), fluorotelomer sulfonate (FTSA), and PFAES analogues were investigated in municipal sewage sludge samples collected around China. Perfluorobutane, perfluorohexane, perfluorooctane, and perfluorodecanesulfonates, 6:2 and 8:2 FTSAs, and the emerging 6:2 Cl-PFAES were detected. Moreover, 8:2 and 10:2 Cl-PFAESs were identified for the first time as new polyfluorinated contaminants using high resolution mass spectrometry. These fluorinated analytes were further quantified with the aid of commercial and laboratory-purified standards. PFOS was the predominant contaminant with a geometric mean (GM) value of 3.19 ng/g dry weight (d.w.), which was subsequently followed by 6:2 Cl-PFAES and 8:2 Cl-PFAES (GM: 2.15 and 0.50 ng/g d.w., respectively). Both 6:2 and 8:2 Cl-PFAES were positively detected as the major components in the F-53B commercial product, and discrete 6:2 Cl-PFAES/8:2 Cl-PFAES ratios in the product and sludge samples might suggest 8:2 Cl-PFAES had enhanced sorption behavior in the sludge due to the increase in hydrophobicity.
  •  
41.
  • Ruan, Ting, et al. (author)
  • Presence and partitioning behavior of polyfluorinated iodine alkanes in environmental matrices around a fluorochemical manufacturing plant : another possible source for perfluorinated carboxylic acids?
  • 2010
  • In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 44:15, s. 5755-5761
  • Journal article (peer-reviewed)abstract
    • The indistinct origins of some ubiquitous perfluorinated alkyl acids have attracted great attention in recent decades. In this present work, even-chained polyfluorinated iodides (PFIs), a group of volatile perfluorinated compounds (PFCs), including four perfluorinated iodine alkanes (FIAs) and three polyfluorinated telomer iodides (FTIs) were confirmed to be present in the environment. A wide concentration range was found for FIAs at 1.41 to 3.08x104 pg/L, and for FTIs at 1.39 to 1.32x103 pg/L in the ambient air collected around a fluorochemical manufacturing plant in Shandong province, northern China. Whereas for surface soils, most of these PFIs were below detection limits and only small amounts of analytes with higher carbon chain (such as perfluorododecyl iodide and 1H,1H,2H,2H-perfluorodecyl iodide, 16.6-499 pg/g) could be sporadically detected. The presence of the PFIs in different environmental matrices in the investigated area and calculated vapor pressures (0.095-20.4 Torr) verify that they can be considered as volatile organic chemicals and easily be released into the atmosphere. Together with reported degradation ability and long-range transport potential, the identification of these PFIs indicates that unintentional release during the telomer reaction process might also be another route for the formation and distribution of certain polyfluorinated alcohols, aldehydes, and carboxylic acid derivatives under oxidative conditions in the environment.
  •  
42.
  • Ruan, Ting, et al. (author)
  • Trace determination of airborne polyfluorinated iodine alkanes using multisorbent thermal desorption/gas chromatography/high resolution mass spectrometry
  • 2010
  • In: Journal of Chromatography A. - : Elsevier. - 0021-9673 .- 1873-3778. ; 1217:26, s. 4439-4447
  • Journal article (peer-reviewed)abstract
    • A novel gas chromatography/high resolution mass spectrometry method coupled with multisorbent thermal desorption cartridges has been developed for the determination of volatile neutral polyfluorinated iodine alkanes (PFIs) in airborne samples. It allows, for the first time, simultaneous analysis of four mono-iodized perfluorinated alkanes, three diiodized perfluorinated alkanes and four mono-iodized polyfluorinated telomers in ambient air samples. 3.75 L air sample was passed through a sorbent tube packed with 150 mg of Tenax TA and 200mg of Carbograph 1 TD for analyte adsorption. Important factors during the analysis procedures, such as safe sampling volume, air sampling rate, analyte desorption and transfer strategies, were optimized and good thermal desorption efficiencies were obtained. The method detection limit (MDL) concentration ranged from 0.04 pg/L for 1H,1H,2H,2H-perfluorododecyl iodide to 1.2 pg/L for perfluorohexyl iodide, and instrument response of a seven-point calibration was linear in the range of 10-1000 pg. Travel spike recoveries ranged from 83% to 116%. Small variabilities of less than 36% were obtained near the MDLs and the differences between triplicates were even smaller (2.1-7.3%) at 200 pg spiked level. The method was successfully applied to analyze ambient air samples collected near a point source, and five PFIs were identified (10.8-85.0 pg/L), with none of the analytes detectable at the background site.
  •  
43.
  • Shang, Hongtao, et al. (author)
  • Bioaccumulation of PCDD/Fs, PCBs and PBDEs by earthworms in field soils of an E-waste dismantling area in China
  • 2013
  • In: Environment International. - : Elsevier. - 0160-4120 .- 1873-6750. ; 54, s. 50-58
  • Journal article (peer-reviewed)abstract
    • A total of 60 paired samples of earthworm, corresponding soil and wormcast were collected to investigate the bioaccumulation tendency of polychlorinated dibenzo-p-dioxins/dibenzofurans (PCDD/Fs), polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) in earthworms from a typical E-waste dismantling area in east China. Significant correlations were observed for the total concentrations among different matrix types except for PCDD/Fs in soil and earthworm. The bioaccumulation tendency showed some differences among the contaminants. Calculated biota-soil accumulation factors (BSAFs) indicated that PCBs and PBDEs had higher bioaccumulation potential compared to PCDD/Fs, which was somewhat different from laboratory studies. The plot of mean BSAFs versus log Kow values for PCBs and PBDEs was well fitted by a second-order polynomial with the maximum BSAF at approximately log Kow of 6.5. While for PCDD/Fs, only a slightly decreasing trend was observed with increasing log Kow. Composition analysis indicated that tetra-, penta- and hexa-halogenated homologs had higher bioaccumulation levels, indicating that medium-halogenated congeners with log Kow around 6.5 are more easily accumulated by earthworms. Furthermore, the ratios of BDE-47/-99 and BDE-99/-100 showed some discrepancies with the technical products and other biotic species, suggesting different bioaccumulation potential of PBDEs in earthworm.
  •  
44.
  • Shang, Hongtao, et al. (author)
  • The presence of polychlorinated biphenyls in yellow pigment products in China with emphasis on 3,3'-dichlorobiphenyl (PCB 11)
  • 2014
  • In: Chemosphere. - : Elsevier. - 0045-6535 .- 1879-1298. ; 98, s. 44-50
  • Journal article (peer-reviewed)abstract
    • A non-Aroclor PCB congener, 3,3'-dichlorobiphenyl (PCB 11) has recently attracted wide concerns because of its environmental ubiquity and specific sources potentially associated with yellow pigment production. In order to investigate PCB 11 and other PCBs in the yellow pigment products, 24 yellow pigment samples were collected from three different manufacturing plants in China. ∑20PCBs and PCB 11 were in the range of 50.7-9.19×10(5) ng g−1 and 41.7-9.18×105 ng g−1, respectively, which was much higher than those reported in previous study. The corresponding TEQ values ranged between 0.16 and 4.21×103 ng WHO2005-TEQ kg−1. The contribution of PCB 11 to ∑20PCBs reached up to 85.5% (median value) followed by PCB 28, PCB 77, and PCB 52 with contributions of 10.5%, 6.70%, and 5.40%, respectively. Significant differences were observed for PCB 11 concentrations among the different types of yellow pigment from the same plant and among the same sample types from different plants. The PCB 11 concentrations in diarylide yellow pigments produced from 3,3'-dichlorbenzidine were the highest in all the samples. It demonstrates that yellow pigment is a significant source not only for the widespread pollution of PCB 11 but also for other PCBs, especially for the lower chlorinated congeners.
  •  
45.
  • Song, Shanjun, et al. (author)
  • Distribution and preliminary exposure assessment of bisphenol AF (BPAF) in various environmental matrices around a manufacturing plant in China
  • 2012
  • In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 46:24, s. 13136-13143
  • Journal article (peer-reviewed)abstract
    • Increasing attention has been paid to bisphenol A and bisphenol (BP) analogues due to high production volumes, wide usage and potential adverse effects. Bisphenol AF (BPAF) is considered a new bisphenol analogue which is used as raw material in plastic industry, but little is known about its occurrence in the environment and the potential associated risk. In this work, BPAF levels and environmental distribution were reported in samples collected around a manufacturing plant and a preliminary exposure risk assessment to local residents was conducted. BPAF was detected in most of the samples, with levels in river ranging between
  •  
46.
  • Song, Shanjun, et al. (author)
  • Occurrence and profiles of bisphenol analogues in municipal sewage sludge in China
  • 2014
  • In: Environmental Pollution. - : Elsevier. - 0269-7491 .- 1873-6424. ; 186, s. 14-19
  • Journal article (peer-reviewed)abstract
    • Extensive use of bisphenol A and its analogues has caused increasing concern over the potential adverse health impacts of these chemicals. In this study, the presence and profiles of 13 bisphenols (BPs) were investigated in 52 municipal sewage sludge samples collected from 30 cities in China. Tetrabromobisphenol A was the most frequently observed analogue (geometric mean: 20.5 ng/g dw). Bisphenol A (4.69 ng/g dw), bisphenol S (3.02 ng/g dw), and bisphenol F (3.84 ng/g dw) were found with similar frequency. Other BP analogues such as tetrachlorobisphenol A, bisphenol AF, bisphenol E, and dihydroxybiphenyl were identified for the first time in sewage sludge in China. Significant correlations were found among BP concentrations, but no relationships were found with wastewater treatment plant characteristics. Profiles of the relative estradiol equivalents suggested that the estrogenic potential of BP mixtures may be associated with the occurrence and contributions of specific analogues.
  •  
47.
  • Song, Shanjun, et al. (author)
  • Occurrence and removal of benzotriazole ultraviolet stabilizers in a wastewater treatment plant in China
  • 2014
  • In: Environmental Science. - : Royal Society of Chemistry. - 2050-7887 .- 2050-7895. ; 16:5, s. 1076-1082
  • Journal article (peer-reviewed)abstract
    • Benzotriazole ultraviolet stabilizers (BZT-UVs) have previously been found in sludge from wastewater treatment plants (WWTPs), which might be potential sources of BZT-UVs to the surrounding environment. In this work, the occurrence and fate of seven emerging 2-hydroxyphenyl substituted BZT-UVs were investigated in a Chinese WWTP. This group of hydrophobic BZT-UVs possess log Kow values ranging from 4.31 to 7.67 which could be associated with their fate in WWTPs. Field samples including 24 h flow composites of influent, effluent and grab sludge samples from different treatment processes were collected and analyzed. Concentrations of BZT-UVs dissolved in aqueous-phases were in the range of 4.88±1.35 (UV-234) to 34.5±12.4 ng L-1 (UV-P) in the primary influent, while only UV-P and UV-328 were detected in the final effluent at concentrations of 10.5±6.59 and 2.74±1.73 ng L-1, respectively. Considering the amount of target BZT-UVs adsorbed to total suspended solids (TSS), the daily mass flux in the primary influent of the WWTP ranged from 22.3 g day(-1) (UV-P, 7.99%) to 74.0 g day-1 (UV-234, 26.5%). Total removal efficiency of the integrated treatment process ranged from 89.7% for UV-P to 99.7% for UV-234 suggesting nearly complete removal. Organic solid sedimentation in primary and secondary clarifiers was the dominant elimination route for BZT-UV analogues, which constituted 96.3% of the total removal efficiency. Advanced treatment (using ultraviolet disinfection) in this plant might further contribute to the high removal efficiencies (ranging from 19.6% to 77.3%).
  •  
48.
  • Sun, Jianteng, et al. (author)
  • Hydroxylated polybrominated diphenyl ethers (OH-PBDEs) in biosolids from municipal wastewater treatment plants in China
  • 2013
  • In: Chemosphere. - : Elsevier. - 0045-6535 .- 1879-1298. ; 90:9, s. 2388-2395
  • Journal article (peer-reviewed)abstract
    • Hydroxylated polybrominated diphenyl ethers (OH-PBDEs) along with methoxylated polybrominated diphenyl ethers (MeO-PBDEs) have been frequently identified as natural compounds in marine environment and also assumed as metabolites of PBDEs. In the present study, nine OH-PBDE, nine MeO-PBDE and 10 PBDE congeners were studied in the sewage sludge collected from 36 municipal wastewater treatment plants (WWTPs) in 27 cities of China. The results suggest that OH-PBDEs and PBDEs are ubiquitous in sewage sludge in China, however, methoxylated PBDEs were not detectable. Composition profiles of detected OH-PBDE congeners were different depending on the sampling location. ΣOH-PBDEs in WWTPs sludge ranged from 0.04 to 2.24 ng g-1 dry weight (mean: 0.35 ng g-1 dry weight). The total amount of the two most prominent congeners (6-OH-BDE-47+2'-OH-BDE-68) accounted for about 53.3-100% of the sum of all six identified congeners. A significant linear relationship was found between 6-OH-BDE-47 and 2'-OH-BDE-68. A distinct geographical distribution of ΣOH-PBDEs was observed with greater concentrations of OH-PBDEs at coastal areas than inland regions in China.
  •  
49.
  • Sun, Jianteng, et al. (author)
  • In vivo metabolism of 2,2',4,4'-tetrabromodiphenyl ether (BDE-47) in young whole pumpkin plant
  • 2013
  • In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 47:8, s. 3701-3707
  • Journal article (peer-reviewed)abstract
    • Polybrominated diphenyl ethers (PBDEs) are widely distributed persistent organic pollutants. In vitro and in vivo research using various animal models have shown that PBDEs might be transformed to hydroxylated PBDEs, but there are few studies on in vivo metabolism of PBDEs by intact whole plants. In this research, pumpkin plants (Cucurbita maxima × C. moschata) were hydroponically exposed to 2,2',4,4'-tetrabromodiphenyl ether (BDE-47). A debromination product (BDE-28) and four hydroxylated metabolites (5-OH-BDE-47, 6-OH-BDE-47, 4'-OH-BDE-49, and 4-OH-BDE-42) were detected in different parts of the whole plant. In addition, 4-methoxylated-2,2',3,4'-tetraBDE (4-MeO-BDE-42) was observed as a methoxylation product. Root exudates in solution were found to play an important role in metabolizing BDE-47 to a specific OH-PBDE: 4'-OH-BDE-49. BDE-28 was found to translocate more easily and accumulate in shoots than BDE-47 due to the lower hydrophobicity and molecular weight. The concentration ratio between metabolites and parent compound BDE-47 was lower for OH-PBDEs than that for both BDE-28 and 4-MeO-BDE-42. The metabolism pathway of BDE-47 in young whole plants was proposed in this study.
  •  
50.
  • Sun, Zhendong, et al. (author)
  • 4-Hexylphenol influences adipogenic differentiation and hepatic lipid accumulation in vitro
  • 2021
  • In: Environmental Pollution. - : Elsevier. - 0269-7491 .- 1873-6424. ; 268:Part A
  • Journal article (peer-reviewed)abstract
    • Finding the potential environmental obesogens is crucial to explain the prevalence of obesity and the related pathologies. Increasing evidence has showed that many chemicals with endocrine disrupting effects can disturb lipid metabolism. Whether 4-hexylphenol (4-HP), a widely-used surfactant and a potential endocrine disrupting chemical (EDC), is associated to influence adipogenesis and hepatic lipid accumulation remained to be elucidated. In this study, both the 3T3-L1 differentiation model and oleic acid (OA)-treated HepG2 cells were used to investigate the effects of 4-HP on lipid metabolism, and the underlying estrogen receptor (ER)-involved mechanism was explored using MVLN assay, molecular docking simulation and the antagonist test. The results based on lipid droplet staining and triglyceride accumulation assay showed that 4-HP treatment promoted the adipogenic differentiation of 3T3-L1 cells and increased hepatic cellular OA accumulation in exposure concentration-dependent manners. The study on the elaborated transcription networks indicated that 4-HP activated peroxisome proliferator-activated receptor γ (PPARγ) as well as the subsequent adipogenic gene program in 3T3-L1 cells. This chemical also induced the increase of OA uptake and decreases of de novo lipogenesis and fatty acid oxidation in HepG2 cells. The agonistic activity of 4-HP in triggering ER-mediated pathway was shown to correlate with its perturbation in lipid metabolism, as evidenced by the enhanced development of mature lipid-laden adipocytes and suppression of excessive hepatic lipid accumulation upon its co-treatment with ER antagonist. Altogether, these findings provide new insights into the potential health impacts of 4-HP exposure as it may relate to obesity and nonalcoholic fatty liver disease.
  •  
Skapa referenser, mejla, bekava och länka
  • Result 1-50 of 100

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view