Affiner votre recherche
Résultats 341-350 de 4,042
Tracking the conversion of nitrogen during pyrolysis of antibiotic mycelial fermentation residues using XPS and TG-FTIR-MS technology Texte intégral
2016
Zhu, Xiangdong | Yang, Shijun | Wang, Liang | Liu, Yuchen | Qian, Feng | Yao, Wenqing | Zhang, Shicheng | Chen, Jianmin
Antibiotic mycelial fermentation residues (AMFRs), which are emerging solid pollutants, have been recognized as hazardous waste in China since 2008. Nitrogen (N), which is an environmental sensitivity element, is largely retained in AMFR samples derived from fermentation substrates. Pyrolysis is a promising technology for the treatment of solid waste. However, the outcomes of N element during the pyrolysis of AMFRs are still unknown. In this study, the conversion of N element during the pyrolysis of AMFRs was tracked using XPS (X-ray photoelectron spectroscopy) and online TG-FTIR-MS (Thermogravimetry-Fourier transform infrared-Mass spectrometry) technology. In the AMFR sample, organic amine-N, pyrrolic-N, protein-N, pyridinic-N, was the main N-containing species. XPS results indicated that pyrrolic-N and pyridinic-N were retained in the AMFR-derived pyrolysis char. More stable species, such as N-oxide and quaternary-N, were also produced in the char. TG-FTIR-MS results indicated that NH3 and HCN were the main gaseous species, and their contents were closely related to the contents of amine-N and protein-N, and pyrrolic-N and pyridinic-N of AMFRs, respectively. Increases in heating rate enhanced the amounts of NH3 and HCN, but had less of an effect on the degradation degree of AMFRs. N-containing organic compounds, including amine-N, nitrile-N and heterocyclic-N, were discerned from the AMFR pyrolysis process. Their release range was extended with increasing of heating rate and carbon content of AMFR sample. This work will help to take appropriate measure to reduce secondary pollution from the treatment of AMFRs.
Afficher plus [+] Moins [-]Shipboard and ground measurements of atmospheric particulate mercury and total mercury in precipitation over the Yellow Sea region Texte intégral
2016
Nguyen, Duc Luong | Kim, Jin Young | Shim, Shang-gyoo | Ghim, Young Sung | Zhang, Xiao-Shan
The first ever shipboard measurements for atmospheric particulate mercury (Hg(p)) over the Yellow Sea and ground measurements for atmospheric Hg(p) and total mercury (THg) in precipitation at the remote sites (Deokjeok and Chengshantou) and the urban sites (Seoul and Ningbo) surrounding the Yellow Sea were carried out during 2007–2008. The Hg(p) regional background concentration of 56.3 ± 55.6 pg m−3 over the Yellow Sea region is much higher than the typical background concentrations of Hg(p) in terrestrial environments (<25 pg m−3) which implies significant impact of anthropogenic mercury emission sources from East Asia. The episodes of highly elevated Hg(p) concentrations at the Korean remote site were influenced through long-range transport from source regions in the Liaoning Province - one of China's most mercury-polluted regions and in the western region of North Korea. Interestingly, wet scavenging of atmospheric Hg(p) is the predominant mechanism regulating concentration of THg in precipitation at the Chinese sites; whereas, wet scavenging of gaseous oxidized mercury (GOM) might play the more important role than that of Hg(p) at the Korean sites. The highest annual wet and dry deposition fluxes of Hg were found at the Ningbo site. The comparison between wet and dry deposition fluxes suggested that dry deposition might play the more important role than wet deposition in Chinese urban areas (source regions); whereas, wet deposition is more important in Korean areas (downwind regions).
Afficher plus [+] Moins [-]Transportation and transformation of mercury in a calcine profile in the Wanshan Mercury Mine, SW China Texte intégral
2016
Yin, Runsheng | Gu, Chunhao | Feng, Xinbin | Zheng, Lirong | Hu, Ningning
Calcination of Hg ores has resulted in serious contamination of mercury (Hg) in the environment. To understand the mobilization of Hg in the calcine pile, the speciation of Hg in a profile of a large calcine pile in the Wanshan Mercury Mine, SW China was investigated using the X-ray absorption spectroscopy (XANES), to understand the mobilization of Hg in the calcine pile. Higher concentrations of Hg were observed at the 30–50 cm depth of the profile, corresponding to a cemented layer. This layer is observed in the entire pile, and was formed due to cementation of calcines. Hg species in calcines include cinnabar (α-HgS), metacinnabar (β-HgS), elemental Hg(0), and minor mercuric chloride (HgCl2), but these Hg species show dramatic changes in the profile. Variations in Hg speciation suggest that extensive mobilization of Hg can occur during weathering processes. We show that the cemented layer can prevent the leaching of Hg and the emission of Hg(0) from the pile. High MeHg concentrations were found near the cemented layer, indicating Hg methylation occurs. This study provides important insights into the environmental risk of Hg in mining areas.
Afficher plus [+] Moins [-]Evergreen or deciduous trees for capturing PAHs from ambient air? A case study Texte intégral
2016
De Nicola, Flavia | Concha Graña, Estefanía | López Mahía, Purificación | Muniategui Lorenzo, Soledad | Prada Rodríguez, Darío | Retuerto, Rubén | Carballeira, Alejo | Aboal, Jesús R. | Fernández, J Ángel
Tree canopies play a key role in the cycling of polycyclic aromatic hydrocarbons (PAHs) in terrestrial ecosystems, as leaves can capture PAHs from the air. In this study, accumulation of PAHs was compared in an evergreen species, P. pinaster, and in a deciduous species, Q. robur, in relation to some physio-morphological characteristics. For this purpose, pine needles and oak leaves collected from different sites across Galicia (NW Spain) were analysed to determine PAH contents, specific leaf area, stomatal density and conductance.Leaves and needles contained similar total amounts of PAHs. The major contribution of particle-bound PAHs in oak (the concentrations of 4- and 5-ring PAHs were two times higher, and those of 6-ring PAHs five times higher in oak than in pine) may be related to the higher specific leaf area (13 and 4 cm2 g−1 dry mass in respectively oak and pine). However, the major contribution of vapor-phase PAHs in pines may be affected by the stomatal conductance (two times higher in pine than in oak). Moreover, an increase in the diameter at breast height of trees led to an increase in accumulation of PAHs, with pine capturing higher amounts of low and medium molecular weight PAHs. The study findings underline the potential role of trees in improving air quality, taking into account the canopy biomass and life cycle.
Afficher plus [+] Moins [-]The effect of lead exposure on fatty acid composition in mouse brain analyzed using pseudo-catalytic derivatization Texte intégral
2016
Jung, Jong-Min | Lee, Jechan | Kim, Ki Hyun | Jang, In Geon | Song, Jae Gwang | Kang, Kyeongjin | Tack, Filip M.G. | Oh, Jeong-Ik | Kwon, Eilhann E. | Kim, Hyung Wook
We performed toxicological study of mice exposed to lead by quantifying fatty acids in brain of the mice. This study suggests that the introduced analytical method had an extremely high tolerance against impurities such as water and extractives; thus, it led to the enhanced resolution in visualizing the spectrum of fatty acid profiles in animal brain. Furthermore, one of the biggest technical advantages achieved in this study was the quantitation of fatty acid methyl ester profiles of mouse brain using a trace amount of sample (e.g., 100 μL mixture). Methanol was screened as the most effective extraction solvent for mouse brain. The behavioral test of the mice before and after lead exposure was conducted to see the effect of lead exposure on fatty acid composition of the mice’ brain. The lead exposure led to changes in disease-related behavior of the mice. Also, the lead exposure induced significant alterations of fatty acid profile (C16:0, C 18:0, and C 18:1) in brain of the mice, implicated in pathology of psychiatric diseases. The alteration of fatty acid profile of brain of the mice suggests that the derivatizing technique can be applicable to most research fields associated with the environmental neurotoxins with better resolution in a short time, as compared to the current protocols for lipid analysis.
Afficher plus [+] Moins [-]Air-sea exchange of gaseous mercury in the East China Sea Texte intégral
2016
Wang, Chunjie | Ci, Zhijia | Wang, Zhangwei | Zhang, Xiaoshan
Two oceanographic cruises were carried out in the East China Sea (ECS) during the summer and fall of 2013. The main objectives of this study are to identify the spatial-temporal distributions of gaseous elemental mercury (GEM) in air and dissolved gaseous mercury (DGM) in surface seawater, and then to estimate the Hg0 flux. The GEM concentration was lower in summer (1.61 ± 0.32 ng m−3) than in fall (2.20 ± 0.58 ng m−3). The back-trajectory analysis revealed that the air masses with high GEM levels during fall largely originated from the land, while the air masses with low GEM levels during summer primarily originated from ocean. The spatial distribution patterns of total Hg (THg), fluorescence, and turbidity were consistent with the pattern of DGM with high levels in the nearshore area and low levels in the open sea. Additionally, the levels of percentage of DGM to THg (%DGM) were higher in the open sea than in the nearshore area, which was consistent with the previous studies. The THg concentration in fall was higher (1.47 ± 0.51 ng l−1) than those of other open oceans. The DGM concentration (60.1 ± 17.6 pg l−1) and Hg0 flux (4.6 ± 3.6 ng m−2 h−1) in summer were higher than those in fall (DGM: 49.6 ± 12.5 pg l−1 and Hg0 flux: 3.6 ± 2.8 ng m−2 h−1). The emission flux of Hg0 from the ECS was estimated to be 27.6 tons yr−1, accounting for ∼0.98% of the global Hg oceanic evasion though the ECS only accounts for ∼0.21% of global ocean area, indicating that the ECS plays an important role in the oceanic Hg cycle.
Afficher plus [+] Moins [-]Origin of inorganic and organic components of PM2.5 in subway stations of Barcelona, Spain Texte intégral
2016
Martins, Vânia | Moreno, Teresa | Minguillón, María Cruz | van Drooge, Barend L. | Reche, Cristina | Amato, F. (Fulvio) | de Miguel, Eladio | Capdevila, Marta | Centelles, Sonia | Querol, X. (Xavier)
Origin of inorganic and organic components of PM2.5 in subway stations of Barcelona, Spain Texte intégral
2016
Martins, Vânia | Moreno, Teresa | Minguillón, María Cruz | van Drooge, Barend L. | Reche, Cristina | Amato, F. (Fulvio) | de Miguel, Eladio | Capdevila, Marta | Centelles, Sonia | Querol, X. (Xavier)
The present work assesses indoor air quality in stations of the Barcelona subway system. PM2.5 concentrations on the platforms of 4 subway stations were measured during two different seasons and the chemical composition was determined. A Positive Matrix Factorization analysis was performed to identify and quantify the contributions of major PM2.5 sources in the subway stations. Mean PM2.5 concentrations varied according to the stations design and seasonal periods. PM2.5 was composed of haematite, carbonaceous aerosol, crustal matter, secondary inorganic compounds, trace elements, insoluble sulphate and halite. Organic compounds such as PAHs, nicotine, levoglucosan and aromatic musk compounds were also identified. Subway PM2.5 source comprised emissions from rails, wheels, catenaries, brake pads and pantographs. The subway source showed different chemical profiles for each station, but was always dominated by Fe. Control actions on the source are important for the achievement of better air quality in the subway environment.
Afficher plus [+] Moins [-]Origin of inorganic and organic components of PM2.5 in subway stations of Barcelona, Spain Texte intégral
2016
Martins, Vânia | Moreno, Teresa | Minguillón, María Cruz | Van Drooge, Barend L. | Reche, Cristina | Amato, Fulvio | de Miguel, Eladio | Capdevila, Marta | Centelles, Sonia | Querol, Xavier | European Commission | Martins, Vânia [0000-0003-2465-5880] | Moreno, Teresa [0000-0003-3235-1027] | Minguillón, María Cruz [0000-0002-5464-0391] | Van Drooge, Barend L. [0000-0002-6434-3390] | Reche, Cristina [0000-0002-3387-3989] | Amato, Fulvio [0000-0003-1546-9154] | Querol, Xavier [0000-0002-6549-9899]
The present work assesses indoor air quality in stations of the Barcelona subway system. PM2.5 concentrations on the platforms of 4 subway stations were measured during two different seasons and the chemical composition was determined. A Positive Matrix Factorization analysis was performed to identify and quantify the contributions of major PM2.5 sources in the subway stations. Mean PM2.5 concentrations varied according to the stations design and seasonal periods. PM2.5 was composed of haematite, carbonaceous aerosol, crustal matter, secondary inorganic compounds, trace elements, insoluble sulphate and halite. Organic compounds such as PAHs, nicotine, levoglucosan and aromatic musk compounds were also identified. Subway PM2.5 source comprised emissions from rails, wheels, catenaries, brake pads and pantographs. The subway source showed different chemical profiles for each station, but was always dominated by Fe. Control actions on the source are important for the achievement of better air quality in the subway environment. © 2015 The Authors. | The present study was supported by the European Union Seventh Framework Programme (FP7/2007-2013) under grant agreement no. 315760 HEXACOMM, the Spanish Ministry of Economy and Competitiveness and FEDER funds ( METRO CGL2012-33066 ), and the IMPROVE LIFE project ( LIFE13 ENV/ES/000263 ). Fulvio Amato is beneficiary of an AXA Research Fund postdoctoral grant. The authors would like to thank the Transports Metropolitans de Barcelona METRO staff who arranged the sampling campaign and contributed actively to this work. Appendix A | Peer reviewed
Afficher plus [+] Moins [-]Uptake, translocation and biotransformation kinetics of BDE-47, 6-OH-BDE-47 and 6-MeO-BDE-47 in maize (Zea mays L.) Texte intégral
2016
This study presents a detailed kinetic investigation on the uptake, acropetal translocation and transformation of BDE-47, 6-OH-BDE-47 and 6-MeO-BDE-47 in maize (Zea mays L.) by hydroponic exposure. Root uptake followed the order: BDE-47 > 6-MeO-BDE-47 > 6-OH-BDE-47, while 6-OH-BDE-47 was the most prone to acropetal translocation. Debromination rates of BDE-47 were 1.31 and 1.46 times greater than the hydroxylation and methoxylation rates, respectively. Transformation from BDE-47 to lower brominated OH/MeO-PBDEs occurred mainly through debromination first followed by hydroxylation or methoxylation. There was no transformation from 6-OH-BDE-47 or 6-MeO-BDE-47 to PBDEs. Methylation rate of 6-OH-BDE-47 was twice as high as that of 6-MeO-BDE-47 hydroxylation, indicating methylation of 6-OH-BDE-47 was easier and more rapid than hydroxylation of 6-MeO-BDE-47. Debromination and isomerization were potential metabolic pathways for 6-OH-BDE-47 and 6-MeO-BDE-47 in maize. This study provides important information for better understanding the mechanism on plant uptake and transformation of PBDEs.
Afficher plus [+] Moins [-]Fractionation of airborne particulate-bound elements in haze-fog episode and associated health risks in a megacity of southeast China Texte intégral
2016
Haze caused by high particulate matter loadings is an important environmental issue. PM2.5 was collected in Nanjing, China, during a severe haze–fog event and clear periods. The particulate-bound elements were chemically fractionated using sequential extractions. The average PM2.5 concentration was 3.4 times higher during haze–fog (96–518 μg/m³) than non-haze fog periods (49–142 μg/m³). Nearly all elements showed significantly higher concentrations during haze–fog than non-haze fog periods. Zn, As, Pb, Cd, Mo and Cu were considered to have higher bioavailability and enrichment degree in the atmosphere. Highly bioavailable fractions of elements were associated with high temperatures. The integrated carcinogenic risk for two possible scenarios to individuals exposed to metals was higher than the accepted criterion of 10⁻⁶, whereas noncarcinogenic risk was lower than the safe level of 1. Residents of a city burdened with haze will incur health risks caused by exposure to airborne metals.
Afficher plus [+] Moins [-]Feeding reduces waterborne Cu bioaccumulation in a marine rabbitfish Siganus oramin Texte intégral
2016
Guo, Zhiqiang | Zhang, Wei | Du, Sen | Zhou, Yanyan | Gao, Na | Zhang, Li | Green, Iain
Waterborne metal uptake has been extensively studied and dietary metal assimilation is increasingly recognized in fish, whilst the interaction between the two uptake routes is largely overlooked. This study compared the waterborne Cu bioaccumulation (⁶⁵Cu as tracer) in a juvenile rabbitfish at different feeding regimes (starvation (SG), feeding normal diet (NDG) or diet supplemented with extra Cu (DCG)) to test the hypothesis that feeding can influence waterborne metal uptake in marine fish. NDG and DCG diet was fed as a single meal and then all fish were exposed to waterborne ⁶⁵Cu for 48 h, during which the time course sampling was conducted to determine ⁶⁵Cu bioaccumulation, chyme flow and dietary Cu assimilation. The results revealed that SG fish accumulated the highest ⁶⁵Cu, followed by NDG (61% of SG), whilst DCG fish accumulated the lowest ⁶⁵Cu (34% of SG). These results suggested a protective effect of feeding against waterborne Cu bioaccumulation. This effect was most notable between 10 min and 16 h when there was chyme in gastrointestinal tract (GT). Dietary Cu assimilation mainly occurred before 16 h after feeding. Waterborne ⁶⁵Cu influx rate in the GT was positively correlated with ⁶⁵Cu contents of chyme in NDG, whereas it was largely negatively correlated with ⁶⁵Cu contents of chyme in DCG. The waterborne Cu uptake in the GT was mainly influenced by the chyme flow and dietary Cu assimilation. Overall, our findings suggested that feeding has an important effect on waterborne metal uptake and that both the feeding status of the fish and the relative metal exposure through water and food should be considered in prediction of the metal bioaccumulation and biomonitoring programs.
Afficher plus [+] Moins [-]