Size Distributions of Polycyclic Aromatic Hydrocarbons and Elemental Carbon. 1. Sampling, Measurement Methods, and Source Characterization

1994 ◽  
Vol 28 (4) ◽  
pp. 555-562 ◽  
Author(s):  
Chandra. Venkataraman ◽  
James M. Lyons ◽  
Sheldon K. Friedlander
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Elemental Carbon ◽  
Measurement Methods ◽  
Size Distributions ◽  
Source Characterization ◽  
Polycyclic Aromatic

scholarly journals Downward fluxes of elemental carbon, metals and polycyclic aromatic hydrocarbons in settling particles from the deep Ionian Sea (NESTOR site), Eastern Mediterranean

2012 ◽  
Vol 9 (12) ◽  
pp. 19165-19197 ◽  
Author(s):  
C. Theodosi ◽  
C. Parinos ◽  
A. Gogou ◽  
A. Kokotos ◽  
S. Stavrakakis ◽  
...  
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Mediterranean Sea ◽  
Aromatic Hydrocarbons ◽  
Elemental Carbon ◽  
Eastern Mediterranean ◽  
Vertical Transport ◽  
Sea Surface ◽  
Ionian Sea ◽  
Eastern Mediterranean Sea ◽  
Polycyclic Aromatic

Abstract. To assess sources and major processes controlling vertical transport of both anthropogenic and natural chemical species in deep basins of the Eastern Mediterranean Sea (SE Ionian Sea, Nestor site), we performed chemical characterization (elemental carbon, major and trace metals and polycyclic aromatic hydrocarbons) of marine sinking particles. Sediment traps were deployed at five successive depths, 700 m, 1200 m, 2000 m, 3200 m and 4300 m from the sea surface, during the period of May 2007 to October 2008. Fluxes of all measured species exhibited minimum values from January to March 2008 and maximum from April to September 2008, with an evident covariance revealing a common and rapid vertical transport mechanism from 700 m down to 4300 m depth. Crustal matter flux from atmospheric deposition plays an important role in the temporal variability of particulate matter with significant contribution from biogenic constituents namely the seasonal succession in the export of planktonic biomass, expressed by particulate organic carbon (POC), carbonates and biogenic Si fluxes (Stavrakakis et al., 2012). Tracers (elemental carbon, retene) of the devastating forest fires occurred in August 2007 in southern Greece, were detected at sediment trap material in all depths with a delay of 15 days at 4300 m, indicating a rapid and well-coupled transport of sinking particulate material between the sea-surface and deep layers of the Eastern Mediterranean Sea. Lateral inputs of pollutants at the deepest trap (4300 m) are probably of importance, due to the influence of deep Adriatic water at the study site.

scholarly journals Effects of Different Water Seasons on the Residual Characteristics and Ecological Risk of Polycyclic Aromatic Hydrocarbons in Sediments from Changdang Lake, China

2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
Author(s):  
Javid Hussain ◽  
Zhenhua Zhao ◽  
Yong Pang ◽  
Liling Xia ◽  
Ittehad Hussain ◽  
...  
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Temporal Distribution ◽  
Impact Factors ◽  
Source Characterization ◽  
Wet Season ◽  
Combustion Source ◽  
Study Results ◽  
Polycyclic Aromatic ◽  
The Impact

The sediments’ samples were collected from Changdang Lake for the concentration of fourteen polycyclic aromatic hydrocarbons in March (dry season), June (wet season), and September (temperate season) 2013. The highest average value of∑PAHswas detected as 295.28 ng/g dw in March, followed by 240.91 ng/g dw in June and 165.81 ng/g dw in September. Source characterization studies based on the analysis of diagnostic ratio (triangular plot method) suggested that the PAHs in sediments from Changdang Lake were mainly from the mixed combustion source of biomass and petroleum, and the origins of PAHs in different sampling sites have a great deal of temporal and spatial variability during different water seasons. Redundancy analysis was applied to identify the impact factors and the possible relationship between PAHs and environmental parameters. The predicted results showed that the main factors impacting PAHs temporal distribution were temperature, dissolved oxygen, pH, and oxidation-reduction potential, while conductivity showed secondary impacts on the PAHs distribution. Risk assessment of PAHs in sediments was carried out based on the US Sediments Quality Guidelines (SQGs). By comparing the present study results with SQGs standard values results showed that the adverse effects are not expected at the present levels of PAHs contamination observed in the sediments from Changdang Lake.

scholarly journals Particle size distribution of nitrated and oxygenated polycyclic aromatic hydrocarbons (NPAHs and OPAHs) on traffic and suburban sites of a European megacity: Paris (France)

2012 ◽  
Vol 12 (18) ◽  
pp. 8877-8887 ◽  
Author(s):  
J. Ringuet ◽  
E. Leoz-Garziandia ◽  
H. Budzinski ◽  
E. Villenave ◽  
A. Albinet
Keyword(s):  
Particle Size ◽  
Polycyclic Aromatic Hydrocarbons ◽  
Size Distribution ◽  
Aromatic Hydrocarbons ◽  
Size Distributions ◽  
Particle Size Distributions ◽  
Oxygenated Polycyclic Aromatic Hydrocarbons ◽  
Polycyclic Aromatic ◽  
Traffic Site ◽  
Suburban Site

Abstract. The size distribution of particulate nitrated and oxygenated polycyclic aromatic hydrocarbons (NPAHs and OPAHs) was determined during two field campaigns at a traffic site in summer 2010 and at a suburban site during the MEGAPOLI (Megacities: Emissions, urban, regional and Global Atmospheric POLlution and climate effects, and Integrated tools for assessment and mitigation) experiment in summer 2009. Both, OPAHs and NPAHs were strongly associated (>85%) to fine particles (Dp< 2.5 μm) increasing the interest of their study on a sanitary point of view. Results showed really different NPAH and OPAH particle size distributions between both sites. At traffic site, clearly bimodal (notably for NPAHs) particle size distributions (Dp = 0.14 and 1.4 μm) were observed, while the particle size distributions were more scattered at the suburban site, especially for OPAHs. Bimodal particle size distribution observed at traffic site for the NPAH could be assigned to the vehicle emissions and the particle resuspension. Broadest distribution observed at the suburban site could be attributed to the mass transfer of compounds by volatilization/sorption processes during the transport of particles in the atmosphere. Results also showed that the combination of the study of particle size distributions applied to marker compounds (primary: 1-nitropyrene; secondary: 2-nitrofluoranthene) and to NPAH or OPAH chemical profiles bring some indications on their primary and/or secondary origin. Indeed, 1,4-anthraquinone seemed only primary emitted by vehicles while 7-nitrobenz[a]anthracene, benz[a]antracen7,12-dione and benzo[b]fluorenone seemed secondarily formed in the atmosphere.

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