Control of denitrification in a septage-treating artificial wetland: the dual role of particulate organic carbon

2002 ◽  
Vol 36 (17) ◽  
pp. 4415-4427 ◽  
Author(s):  
M.Robert Hamersley ◽  
Brian L Howes
2014 ◽  
Vol 14 (19) ◽  
pp. 10439-10464 ◽  
Author(s):  
W. Ait-Helal ◽  
A. Borbon ◽  
S. Sauvage ◽  
J. A. de Gouw ◽  
A. Colomb ◽  
...  

Abstract. Measurements of gaseous and particulate organic carbon were performed during the MEGAPOLI experiments, in July 2009 and January–February 2010, at the SIRTA observatory in suburban Paris. Measurements comprise primary and secondary volatile organic compounds (VOCs), of both anthropogenic and biogenic origins, including C12–C16 n-alkanes of intermediate volatility (IVOCs), suspected to be efficient precursors of secondary organic aerosol (SOA). The time series of gaseous carbon are generally consistent with times series of particulate organic carbon at regional scale, and are clearly affected by meteorology and air mass origin. Concentration levels of anthropogenic VOCs in urban and suburban Paris were surprisingly low (2–963 ppt) compared to other megacities worldwide and to rural continental sites. Urban enhancement ratios of anthropogenic VOC pairs agree well between the urban and suburban Paris sites, showing the regional extent of anthropogenic sources of similar composition. Contrary to other primary anthropogenic VOCs (aromatics and alkanes), IVOCs showed lower concentrations in winter (< 5 ppt) compared to summer (13–27 ppt), which cannot be explained by the gas-particle partitioning theory. Higher concentrations of most oxygenated VOCs in winter (18–5984 ppt) suggest their dominant primary anthropogenic origin. The respective role of primary anthropogenic gaseous compounds in regional SOA formation was investigated by estimating the SOA mass concentration expected from the anthropogenic VOCs and IVOCs (I / VOCs) measured at SIRTA. From an integrated approach based on emission ratios and SOA yields, 38 % of the SOA measured at SIRTA is explained by the measured concentrations of I / VOCs, with a 2% contribution by C12–C16 n-alkane IVOCs. From the results of an alternative time-resolved approach, the average IVOC contribution to SOA formation is estimated to be 7%, which is half of the average contribution of the traditional aromatic compounds (15%). Both approaches, which are based on in situ observations of particular I / VOCs, emphasize the importance of the intermediate volatility compounds in the SOA formation, and support previous results from chamber experiments and modeling studies. They also support the need to make systematic the IVOCs' speciated measurement during field campaigns.


2009 ◽  
Vol 55 (1) ◽  
pp. 161-171 ◽  
Author(s):  
Robert A. Wheatcroft ◽  
Miguel A. Goñ i ◽  
Jeff A. Hatten ◽  
Gregory B. Pasternack ◽  
Jonathan A. Warrick

2021 ◽  
pp. 126826
Author(s):  
Elisa Terzaghi ◽  
Giuseppe Raspa ◽  
Elisabetta Zanardini ◽  
Cristiana Morosini ◽  
Simone Anelli ◽  
...  

2014 ◽  
Vol 14 (4) ◽  
pp. 4841-4904 ◽  
Author(s):  
W. Ait-Helal ◽  
A. Borbon ◽  
S. Sauvage ◽  
J. A. de Gouw ◽  
A. Colomb ◽  
...  

Abstract. Measurements of gaseous and particulate organic carbon were performed during the MEGAPOLI experiments, in July 2009 and January–February 2010, at the SIRTA observatory in sub-urban Paris. Measurements of primary and secondary volatile organic compounds (VOCs), of both anthropogenic and biogenic origins, including for the first time C12-C16 n-alkanes of intermediate volatility (IVOCs), suspected to be efficient precursors of secondary organic aerosol (SOA). The time series of gaseous carbon are generally consistent with times series of particulate organic carbon at regional scales and are clearly affected by meteorology and air mass origin. Concentration levels of anthropogenic VOCs in urban and sub-urban Paris were surprisingly low (2–963 ppt) compared to other megacities worldwide and to rural continental sites. Urban enhancement ratios of anthropogenic VOC pairs agree well between the urban and sub-urban Paris sites, showing the regional extent of anthropogenic sources of similar composition. Contrary to other primary anthropogenic VOCs (aromatics and alkanes), IVOCs showed lower concentrations in winter (< 5 ppt) compared to summer (13–27 ppt) in agreement with a gas-particle partitioning in favor of their transfer to the particle phase in winter. Higher concentrations of most oxygenated VOCs in winter (18–5984 ppt) suggest their dominant primary anthropogenic origin. The respective role of primary anthropogenic gaseous compounds in regional SOA formation was investigated by estimating the SOA mass concentration expected from the anthropogenic VOCs and IVOCs (I / VOCs) measured at SIRTA. From an approach based on emissions inferred from the I / VOC concentrations times the SOA formation yields', the so-called integrated approach conducted in this study, 46% of the SOA measured at SIRTA is explained by our measured concentrations of I / VOC, with 10% explained by only C12-C16 IVOCs. From results of an alternative time-resolved approach, the explained variability of the SOA concentrations is improved when the IVOCs are taken into account. Both approaches, which are based on ambient measurements of particular I / VOCs, emphasize the importance of the intermediate volatility compounds in the SOA formation, and support previous results from chamber experiments and modeling studies. The approaches results support the need to make systematic the IVOCs speciated measurement during field campaigns.


2014 ◽  
Vol 122 (03) ◽  
Author(s):  
A Chatzigeorgiou ◽  
R Garcia-Martin ◽  
KJ Chung ◽  
I Alexaki ◽  
A Klotzsche-von Ameln ◽  
...  

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