The evolution of photochemical smog in a power plant plume
The evolution of photochemical smog in a plant plume was investigated with the aid of an instrumented helicopter. Air samples were taken in the plume of the Cumberland Power Plant, located in central Tennessee, during the afternoon of 16 July 1995 as part of the Southern Oxidants Study – Nashville M...
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Veröffentlicht in: | Atmospheric environment (1994) 1999-08, Vol.33 (18), p.3023-3036 |
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container_title | Atmospheric environment (1994) |
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creator | Luria, Menachem Valente, Ralph J. Tanner, Roger L. Gillani, Noor V. Imhoff, Robert E. F. Mueller, Stephen Olszyna, Kenneth J. Meagher, James F. |
description | The evolution of photochemical smog in a plant plume was investigated with the aid of an instrumented helicopter. Air samples were taken in the plume of the Cumberland Power Plant, located in central Tennessee, during the afternoon of 16 July 1995 as part of the Southern Oxidants Study – Nashville Middle Tennessee Ozone Study. Twelve cross-wind air sampling traverses were made at six distance groups from 35 to 116
km from the source. During the sampling period the winds were from the west–northwest and the plume drifted towards the city of Nashville TN. Ten of the traverses were made upwind of the city, where the power plant plume was isolated, and two traverses downwind of the city when the plumes were possibly mixed. The results revealed that even six hours after the release, excess ozone production was limited to the edges of the plume. Only when the plume was sufficiently dispersed, but still upwind of Nashville, was excess ozone (up to 109 ppbv, 50–60
ppbv above background levels) produced in the center of the plume. The concentrations image of the plume and a Lagrangian particle model suggests that portions of the power plant plume mixed with the urban plume. The mixed urban power plant plume began to regenerate O
3 that peaked at 120
ppbv at a short distance (15–25
km) downwind of Nashville. Ozone productivity (the ratio of excess O
3 to NO
y
and NO
z
) in the isolated plume was significantly lower compared with that found in the city plume. The production of nitrate, a chain termination product, was significantly higher in the power plant plume compared to the mixed plume, indicating shorter chain length of the photochemical smog chain reaction mechanism. |
doi_str_mv | 10.1016/S1352-2310(99)00072-2 |
format | Article |
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km from the source. During the sampling period the winds were from the west–northwest and the plume drifted towards the city of Nashville TN. Ten of the traverses were made upwind of the city, where the power plant plume was isolated, and two traverses downwind of the city when the plumes were possibly mixed. The results revealed that even six hours after the release, excess ozone production was limited to the edges of the plume. Only when the plume was sufficiently dispersed, but still upwind of Nashville, was excess ozone (up to 109 ppbv, 50–60
ppbv above background levels) produced in the center of the plume. The concentrations image of the plume and a Lagrangian particle model suggests that portions of the power plant plume mixed with the urban plume. The mixed urban power plant plume began to regenerate O
3 that peaked at 120
ppbv at a short distance (15–25
km) downwind of Nashville. Ozone productivity (the ratio of excess O
3 to NO
y
and NO
z
) in the isolated plume was significantly lower compared with that found in the city plume. The production of nitrate, a chain termination product, was significantly higher in the power plant plume compared to the mixed plume, indicating shorter chain length of the photochemical smog chain reaction mechanism.</description><identifier>ISSN: 1352-2310</identifier><identifier>EISSN: 1873-2844</identifier><identifier>DOI: 10.1016/S1352-2310(99)00072-2</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Applied sciences ; Atmospheric pollution ; Chemical composition and interactions. Ionic interactions and processes ; Combustion and energy production ; Earth, ocean, space ; Exact sciences and technology ; External geophysics ; Meteorology ; Nitric acid and nitrate ; Ozone ; Pollution ; Pollution sources. Measurement results ; Power plant plume ; USA, Tennessee</subject><ispartof>Atmospheric environment (1994), 1999-08, Vol.33 (18), p.3023-3036</ispartof><rights>1999</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c495t-f930224870d83685656a8da8dc487a83ab624c55817e1487b2e6896c067bd4423</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1352231099000722$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27902,27903,65308</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1774044$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Luria, Menachem</creatorcontrib><creatorcontrib>Valente, Ralph J.</creatorcontrib><creatorcontrib>Tanner, Roger L.</creatorcontrib><creatorcontrib>Gillani, Noor V.</creatorcontrib><creatorcontrib>Imhoff, Robert E.</creatorcontrib><creatorcontrib>F. Mueller, Stephen</creatorcontrib><creatorcontrib>Olszyna, Kenneth J.</creatorcontrib><creatorcontrib>Meagher, James F.</creatorcontrib><title>The evolution of photochemical smog in a power plant plume</title><title>Atmospheric environment (1994)</title><description>The evolution of photochemical smog in a plant plume was investigated with the aid of an instrumented helicopter. Air samples were taken in the plume of the Cumberland Power Plant, located in central Tennessee, during the afternoon of 16 July 1995 as part of the Southern Oxidants Study – Nashville Middle Tennessee Ozone Study. Twelve cross-wind air sampling traverses were made at six distance groups from 35 to 116
km from the source. During the sampling period the winds were from the west–northwest and the plume drifted towards the city of Nashville TN. Ten of the traverses were made upwind of the city, where the power plant plume was isolated, and two traverses downwind of the city when the plumes were possibly mixed. The results revealed that even six hours after the release, excess ozone production was limited to the edges of the plume. Only when the plume was sufficiently dispersed, but still upwind of Nashville, was excess ozone (up to 109 ppbv, 50–60
ppbv above background levels) produced in the center of the plume. The concentrations image of the plume and a Lagrangian particle model suggests that portions of the power plant plume mixed with the urban plume. The mixed urban power plant plume began to regenerate O
3 that peaked at 120
ppbv at a short distance (15–25
km) downwind of Nashville. Ozone productivity (the ratio of excess O
3 to NO
y
and NO
z
) in the isolated plume was significantly lower compared with that found in the city plume. The production of nitrate, a chain termination product, was significantly higher in the power plant plume compared to the mixed plume, indicating shorter chain length of the photochemical smog chain reaction mechanism.</description><subject>Applied sciences</subject><subject>Atmospheric pollution</subject><subject>Chemical composition and interactions. Ionic interactions and processes</subject><subject>Combustion and energy production</subject><subject>Earth, ocean, space</subject><subject>Exact sciences and technology</subject><subject>External geophysics</subject><subject>Meteorology</subject><subject>Nitric acid and nitrate</subject><subject>Ozone</subject><subject>Pollution</subject><subject>Pollution sources. 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Measurement results</topic><topic>Power plant plume</topic><topic>USA, Tennessee</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luria, Menachem</creatorcontrib><creatorcontrib>Valente, Ralph J.</creatorcontrib><creatorcontrib>Tanner, Roger L.</creatorcontrib><creatorcontrib>Gillani, Noor V.</creatorcontrib><creatorcontrib>Imhoff, Robert E.</creatorcontrib><creatorcontrib>F. 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Mueller, Stephen</au><au>Olszyna, Kenneth J.</au><au>Meagher, James F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The evolution of photochemical smog in a power plant plume</atitle><jtitle>Atmospheric environment (1994)</jtitle><date>1999-08-01</date><risdate>1999</risdate><volume>33</volume><issue>18</issue><spage>3023</spage><epage>3036</epage><pages>3023-3036</pages><issn>1352-2310</issn><eissn>1873-2844</eissn><abstract>The evolution of photochemical smog in a plant plume was investigated with the aid of an instrumented helicopter. Air samples were taken in the plume of the Cumberland Power Plant, located in central Tennessee, during the afternoon of 16 July 1995 as part of the Southern Oxidants Study – Nashville Middle Tennessee Ozone Study. Twelve cross-wind air sampling traverses were made at six distance groups from 35 to 116
km from the source. During the sampling period the winds were from the west–northwest and the plume drifted towards the city of Nashville TN. Ten of the traverses were made upwind of the city, where the power plant plume was isolated, and two traverses downwind of the city when the plumes were possibly mixed. The results revealed that even six hours after the release, excess ozone production was limited to the edges of the plume. Only when the plume was sufficiently dispersed, but still upwind of Nashville, was excess ozone (up to 109 ppbv, 50–60
ppbv above background levels) produced in the center of the plume. The concentrations image of the plume and a Lagrangian particle model suggests that portions of the power plant plume mixed with the urban plume. The mixed urban power plant plume began to regenerate O
3 that peaked at 120
ppbv at a short distance (15–25
km) downwind of Nashville. Ozone productivity (the ratio of excess O
3 to NO
y
and NO
z
) in the isolated plume was significantly lower compared with that found in the city plume. The production of nitrate, a chain termination product, was significantly higher in the power plant plume compared to the mixed plume, indicating shorter chain length of the photochemical smog chain reaction mechanism.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/S1352-2310(99)00072-2</doi><tpages>14</tpages></addata></record> |
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subjects | Applied sciences Atmospheric pollution Chemical composition and interactions. Ionic interactions and processes Combustion and energy production Earth, ocean, space Exact sciences and technology External geophysics Meteorology Nitric acid and nitrate Ozone Pollution Pollution sources. Measurement results Power plant plume USA, Tennessee |
title | The evolution of photochemical smog in a power plant plume |
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