Reactive uptake of glyoxal by particulate matter
The uptake of gaseous glyoxal onto particulate matter has been studied in laboratory experiments under conditions relevant to the ambient atmosphere using an aerosol mass spectrometer. The growth rates and reactive uptake coefficients, γ, were derived by fitting a model of particle growth to the exp...
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Veröffentlicht in: | Journal of Geophysical Research. D. Atmospheres 2005-05, Vol.110 (D10), p.D10304.1-n/a |
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creator | Liggio, John Li, Shao-Meng McLaren, Robert |
description | The uptake of gaseous glyoxal onto particulate matter has been studied in laboratory experiments under conditions relevant to the ambient atmosphere using an aerosol mass spectrometer. The growth rates and reactive uptake coefficients, γ, were derived by fitting a model of particle growth to the experimental data. Organic growth rates varied from 1.05 × 10−11 to 23.1 × 10−11 μg particle−1 min−1 in the presence of ∼5 ppb glyoxal. Uptake coefficients (γ) of glyoxal varied from 8.0 × 10−4 to 7.3 × 10−3 with a median γ = 2.9 × 10−3, observed for (NH4)2SO4 seed aerosols at 55% relative humidity. Increased γ values were related to increased particle acidity, indicating that acid catalysis played a role in the heterogeneous mechanism. Experiments conducted at very low relative humidity, with the potential to be highly acidic, resulted in very low reactive uptake. These uptake coefficients indicated that the heterogeneous loss of glyoxal in the atmosphere is at least as important as gas phase loss mechanisms, including photolysis and reaction with hydroxyl radicals. Glyoxal lifetime due to heterogeneous reactions under typical ambient conditions was estimated to be τhet = 5–287 min. In rural and remote areas the glyoxal uptake can lead to 5–257 ng m−3 of secondary organic aerosols in 8 hours, consistent with recent ambient measurements. |
doi_str_mv | 10.1029/2004JD005113 |
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The growth rates and reactive uptake coefficients, γ, were derived by fitting a model of particle growth to the experimental data. Organic growth rates varied from 1.05 × 10−11 to 23.1 × 10−11 μg particle−1 min−1 in the presence of ∼5 ppb glyoxal. Uptake coefficients (γ) of glyoxal varied from 8.0 × 10−4 to 7.3 × 10−3 with a median γ = 2.9 × 10−3, observed for (NH4)2SO4 seed aerosols at 55% relative humidity. Increased γ values were related to increased particle acidity, indicating that acid catalysis played a role in the heterogeneous mechanism. Experiments conducted at very low relative humidity, with the potential to be highly acidic, resulted in very low reactive uptake. These uptake coefficients indicated that the heterogeneous loss of glyoxal in the atmosphere is at least as important as gas phase loss mechanisms, including photolysis and reaction with hydroxyl radicals. Glyoxal lifetime due to heterogeneous reactions under typical ambient conditions was estimated to be τhet = 5–287 min. In rural and remote areas the glyoxal uptake can lead to 5–257 ng m−3 of secondary organic aerosols in 8 hours, consistent with recent ambient measurements.</description><identifier>ISSN: 0148-0227</identifier><identifier>EISSN: 2156-2202</identifier><identifier>DOI: 10.1029/2004JD005113</identifier><language>eng</language><publisher>Washington, DC: Blackwell Publishing Ltd</publisher><subject>aerosols ; Earth sciences ; Earth, ocean, space ; Exact sciences and technology ; glyoxal ; uptake coefficient</subject><ispartof>Journal of Geophysical Research. D. Atmospheres, 2005-05, Vol.110 (D10), p.D10304.1-n/a</ispartof><rights>Copyright 2005 by the American Geophysical Union.</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4823-c33469a9ef998d048e7f49d2cecfabcab76fa28fe2e3fe1b07e7d475f89ca1e83</citedby><cites>FETCH-LOGICAL-c4823-c33469a9ef998d048e7f49d2cecfabcab76fa28fe2e3fe1b07e7d475f89ca1e83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1029%2F2004JD005113$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1029%2F2004JD005113$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,11514,27924,27925,45574,45575,46409,46468,46833,46892</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16912683$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Liggio, John</creatorcontrib><creatorcontrib>Li, Shao-Meng</creatorcontrib><creatorcontrib>McLaren, Robert</creatorcontrib><title>Reactive uptake of glyoxal by particulate matter</title><title>Journal of Geophysical Research. D. Atmospheres</title><addtitle>J. Geophys. Res</addtitle><description>The uptake of gaseous glyoxal onto particulate matter has been studied in laboratory experiments under conditions relevant to the ambient atmosphere using an aerosol mass spectrometer. The growth rates and reactive uptake coefficients, γ, were derived by fitting a model of particle growth to the experimental data. Organic growth rates varied from 1.05 × 10−11 to 23.1 × 10−11 μg particle−1 min−1 in the presence of ∼5 ppb glyoxal. Uptake coefficients (γ) of glyoxal varied from 8.0 × 10−4 to 7.3 × 10−3 with a median γ = 2.9 × 10−3, observed for (NH4)2SO4 seed aerosols at 55% relative humidity. Increased γ values were related to increased particle acidity, indicating that acid catalysis played a role in the heterogeneous mechanism. Experiments conducted at very low relative humidity, with the potential to be highly acidic, resulted in very low reactive uptake. These uptake coefficients indicated that the heterogeneous loss of glyoxal in the atmosphere is at least as important as gas phase loss mechanisms, including photolysis and reaction with hydroxyl radicals. Glyoxal lifetime due to heterogeneous reactions under typical ambient conditions was estimated to be τhet = 5–287 min. In rural and remote areas the glyoxal uptake can lead to 5–257 ng m−3 of secondary organic aerosols in 8 hours, consistent with recent ambient measurements.</description><subject>aerosols</subject><subject>Earth sciences</subject><subject>Earth, ocean, space</subject><subject>Exact sciences and technology</subject><subject>glyoxal</subject><subject>uptake coefficient</subject><issn>0148-0227</issn><issn>2156-2202</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNp9kM1OAjEURhujiQTZ-QCz0ZWj_Zu2szSgo0gwIRiXzaXcmpGBwXZQeHshEHXl3dzNOWfxEXLO6DWjPL_hlMp-j9KMMXFEWpxlKuWc8mPSokyalHKuT0knxne6PZkpSVmL0BGCa8pPTFbLBmaY1D55qzb1GqpkskmWEJrSrSpoMJlD02A4Iyceqoidw2-Tl_u7cfchHTwXj93bQeqk4SJ1QkiVQ44-z82USoPay3zKHToPEwcTrTxw45Gj8MgmVKOeSp15kztgaESbXO67y1B_rDA2dl5Gh1UFC6xX0TKtuJJGbcGrPehCHWNAb5ehnEPYWEbtbhn7d5ktfnHoQnRQ-QALV8ZfR-WMK7PjxJ77Kivc_Nu0_WLUY0ypnZXurTI2uP6xIMys0kJn9nVY2MI8adaXYzsU33IagAo</recordid><startdate>20050527</startdate><enddate>20050527</enddate><creator>Liggio, John</creator><creator>Li, Shao-Meng</creator><creator>McLaren, Robert</creator><general>Blackwell Publishing Ltd</general><general>American Geophysical Union</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TG</scope><scope>KL.</scope></search><sort><creationdate>20050527</creationdate><title>Reactive uptake of glyoxal by particulate matter</title><author>Liggio, John ; Li, Shao-Meng ; McLaren, Robert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4823-c33469a9ef998d048e7f49d2cecfabcab76fa28fe2e3fe1b07e7d475f89ca1e83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>aerosols</topic><topic>Earth sciences</topic><topic>Earth, ocean, space</topic><topic>Exact sciences and technology</topic><topic>glyoxal</topic><topic>uptake coefficient</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liggio, John</creatorcontrib><creatorcontrib>Li, Shao-Meng</creatorcontrib><creatorcontrib>McLaren, Robert</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><jtitle>Journal of Geophysical Research. D. Atmospheres</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liggio, John</au><au>Li, Shao-Meng</au><au>McLaren, Robert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reactive uptake of glyoxal by particulate matter</atitle><jtitle>Journal of Geophysical Research. D. Atmospheres</jtitle><addtitle>J. Geophys. Res</addtitle><date>2005-05-27</date><risdate>2005</risdate><volume>110</volume><issue>D10</issue><spage>D10304.1</spage><epage>n/a</epage><pages>D10304.1-n/a</pages><issn>0148-0227</issn><eissn>2156-2202</eissn><abstract>The uptake of gaseous glyoxal onto particulate matter has been studied in laboratory experiments under conditions relevant to the ambient atmosphere using an aerosol mass spectrometer. The growth rates and reactive uptake coefficients, γ, were derived by fitting a model of particle growth to the experimental data. Organic growth rates varied from 1.05 × 10−11 to 23.1 × 10−11 μg particle−1 min−1 in the presence of ∼5 ppb glyoxal. Uptake coefficients (γ) of glyoxal varied from 8.0 × 10−4 to 7.3 × 10−3 with a median γ = 2.9 × 10−3, observed for (NH4)2SO4 seed aerosols at 55% relative humidity. Increased γ values were related to increased particle acidity, indicating that acid catalysis played a role in the heterogeneous mechanism. Experiments conducted at very low relative humidity, with the potential to be highly acidic, resulted in very low reactive uptake. These uptake coefficients indicated that the heterogeneous loss of glyoxal in the atmosphere is at least as important as gas phase loss mechanisms, including photolysis and reaction with hydroxyl radicals. Glyoxal lifetime due to heterogeneous reactions under typical ambient conditions was estimated to be τhet = 5–287 min. In rural and remote areas the glyoxal uptake can lead to 5–257 ng m−3 of secondary organic aerosols in 8 hours, consistent with recent ambient measurements.</abstract><cop>Washington, DC</cop><pub>Blackwell Publishing Ltd</pub><doi>10.1029/2004JD005113</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | aerosols Earth sciences Earth, ocean, space Exact sciences and technology glyoxal uptake coefficient |
title | Reactive uptake of glyoxal by particulate matter |
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