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Secondary Organic Aerosol Formation and Organic Nitrate Yield from NO3 Oxidation of Biogenic Hydrocarbons
The secondary organic aerosol (SOA) mass yields from NO3 oxidation of a series of biogenic volatile organic compounds (BVOCs), consisting of five monoterpenes and one sesquiterpene (α-pinene, β-pinene, Δ-3-carene, limonene, sabinene, and β-caryophyllene), were investigated in a series of continuous...
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Published in: | Environmental science & technology 2014-10, Vol.48 (20), p.11944-11953 |
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creator | Fry, Juliane L Draper, Danielle C Barsanti, Kelley C Smith, James N Ortega, John Winkler, Paul M Lawler, Michael J Brown, Steven S Edwards, Peter M Cohen, Ronald C Lee, Lance |
description | The secondary organic aerosol (SOA) mass yields from NO3 oxidation of a series of biogenic volatile organic compounds (BVOCs), consisting of five monoterpenes and one sesquiterpene (α-pinene, β-pinene, Δ-3-carene, limonene, sabinene, and β-caryophyllene), were investigated in a series of continuous flow experiments in a 10 m3 indoor Teflon chamber. By making in situ measurements of the nitrate radical and employing a kinetics box model, we generate time-dependent yield curves as a function of reacted BVOC. SOA yields varied dramatically among the different BVOCs, from zero for α-pinene to 38–65% for Δ-3-carene and 86% for β-caryophyllene at mass loading of 10 μg m–3, suggesting that model mechanisms that treat all NO3 + monoterpene reactions equally will lead to errors in predicted SOA depending on each location’s mix of BVOC emissions. In most cases, organonitrate is a dominant component of the aerosol produced, but in the case of α-pinene, little organonitrate and no aerosol is formed. |
doi_str_mv | 10.1021/es502204x |
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By making in situ measurements of the nitrate radical and employing a kinetics box model, we generate time-dependent yield curves as a function of reacted BVOC. SOA yields varied dramatically among the different BVOCs, from zero for α-pinene to 38–65% for Δ-3-carene and 86% for β-caryophyllene at mass loading of 10 μg m–3, suggesting that model mechanisms that treat all NO3 + monoterpene reactions equally will lead to errors in predicted SOA depending on each location’s mix of BVOC emissions. 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Sci. Technol</addtitle><description>The secondary organic aerosol (SOA) mass yields from NO3 oxidation of a series of biogenic volatile organic compounds (BVOCs), consisting of five monoterpenes and one sesquiterpene (α-pinene, β-pinene, Δ-3-carene, limonene, sabinene, and β-caryophyllene), were investigated in a series of continuous flow experiments in a 10 m3 indoor Teflon chamber. By making in situ measurements of the nitrate radical and employing a kinetics box model, we generate time-dependent yield curves as a function of reacted BVOC. SOA yields varied dramatically among the different BVOCs, from zero for α-pinene to 38–65% for Δ-3-carene and 86% for β-caryophyllene at mass loading of 10 μg m–3, suggesting that model mechanisms that treat all NO3 + monoterpene reactions equally will lead to errors in predicted SOA depending on each location’s mix of BVOC emissions. In most cases, organonitrate is a dominant component of the aerosol produced, but in the case of α-pinene, little organonitrate and no aerosol is formed.</description><subject>aerosols</subject><subject>Aerosols - chemistry</subject><subject>Air Pollutants - analysis</subject><subject>Air Pollutants - chemistry</subject><subject>alpha-pinene</subject><subject>Applied sciences</subject><subject>Atmospheric pollution</subject><subject>beta-caryophyllene</subject><subject>beta-pinene</subject><subject>Bridged Bicyclo Compounds - chemistry</subject><subject>carene</subject><subject>Cyclohexenes - chemistry</subject><subject>Earth, ocean, space</subject><subject>emissions</subject><subject>Exact sciences and technology</subject><subject>External geophysics</subject><subject>Kinetics</subject><subject>Limonene</subject><subject>Meteorology</subject><subject>Monoterpenes - chemistry</subject><subject>nitrates</subject><subject>Nitrates - chemistry</subject><subject>oxidation</subject><subject>Particles and aerosols</subject><subject>Pollutants physicochemistry study: properties, effects, reactions, transport and distribution</subject><subject>Pollution</subject><subject>polytetrafluoroethylene</subject><subject>sabinene</subject><subject>Sesquiterpenes - chemistry</subject><subject>Terpenes - chemistry</subject><subject>volatile organic compounds</subject><subject>Volatile Organic Compounds - chemistry</subject><issn>0013-936X</issn><issn>1520-5851</issn><issn>1520-5851</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>N~.</sourceid><recordid>eNpVkUtPHDEQhC2UCDYkB_5A5EskLpO0XzP2BQkQBCTEHhIkcrK8fmyMZmywZxH8-8yKZSGnPvSnqu4qhA4IfCdAyQ9fBVAK_GkHzYig0AgpyAc0AyCsUay93UOfar0DAMpA7qI9KihVFOQMxV_e5uRMecbzsjQpWnzsS665x-e5DGaMOWGT3HZ7HcdiRo__RN87HEoe8PWc4flTdC9wDvgk5qVfwxfPrmRryiKn-hl9DKav_stm7qOb87PfpxfN1fzn5enxVWOYUGNDLOMUwNvWdBCEMiywTjISuGtdANk5Rjq1IFYRJb2SwdsF48oGKxn3tmP76OhF9361GLyzPk0H9_q-xGH6UmcT9f-bFP_qZX7Uky3ngkwChxuBkh9Wvo56iNX6vjfJ51XVdJ2jEly1E_r1vdfW5DXfCfi2AUy1pg_FJBvrGyeVoi2HN87Yqu_yqqQpIk1Ar_vV237ZP3pKljU</recordid><startdate>20141021</startdate><enddate>20141021</enddate><creator>Fry, Juliane L</creator><creator>Draper, Danielle C</creator><creator>Barsanti, Kelley C</creator><creator>Smith, James N</creator><creator>Ortega, John</creator><creator>Winkler, Paul M</creator><creator>Lawler, Michael J</creator><creator>Brown, Steven S</creator><creator>Edwards, Peter M</creator><creator>Cohen, Ronald C</creator><creator>Lee, Lance</creator><general>American Chemical Society</general><scope>N~.</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20141021</creationdate><title>Secondary Organic Aerosol Formation and Organic Nitrate Yield from NO3 Oxidation of Biogenic Hydrocarbons</title><author>Fry, Juliane L ; Draper, Danielle C ; Barsanti, Kelley C ; Smith, James N ; Ortega, John ; Winkler, Paul M ; Lawler, Michael J ; Brown, Steven S ; Edwards, Peter M ; Cohen, Ronald C ; Lee, Lance</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a359t-1c34200ec6a70f59a3f37831f4d6df087d3179b1c9198e98fecb349cfc834ec73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>aerosols</topic><topic>Aerosols - chemistry</topic><topic>Air Pollutants - analysis</topic><topic>Air Pollutants - chemistry</topic><topic>alpha-pinene</topic><topic>Applied sciences</topic><topic>Atmospheric pollution</topic><topic>beta-caryophyllene</topic><topic>beta-pinene</topic><topic>Bridged Bicyclo Compounds - chemistry</topic><topic>carene</topic><topic>Cyclohexenes - chemistry</topic><topic>Earth, ocean, space</topic><topic>emissions</topic><topic>Exact sciences and technology</topic><topic>External geophysics</topic><topic>Kinetics</topic><topic>Limonene</topic><topic>Meteorology</topic><topic>Monoterpenes - chemistry</topic><topic>nitrates</topic><topic>Nitrates - chemistry</topic><topic>oxidation</topic><topic>Particles and aerosols</topic><topic>Pollutants physicochemistry study: properties, effects, reactions, transport and distribution</topic><topic>Pollution</topic><topic>polytetrafluoroethylene</topic><topic>sabinene</topic><topic>Sesquiterpenes - chemistry</topic><topic>Terpenes - chemistry</topic><topic>volatile organic compounds</topic><topic>Volatile Organic Compounds - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fry, Juliane L</creatorcontrib><creatorcontrib>Draper, Danielle C</creatorcontrib><creatorcontrib>Barsanti, Kelley C</creatorcontrib><creatorcontrib>Smith, James N</creatorcontrib><creatorcontrib>Ortega, John</creatorcontrib><creatorcontrib>Winkler, Paul M</creatorcontrib><creatorcontrib>Lawler, Michael J</creatorcontrib><creatorcontrib>Brown, Steven S</creatorcontrib><creatorcontrib>Edwards, Peter M</creatorcontrib><creatorcontrib>Cohen, Ronald C</creatorcontrib><creatorcontrib>Lee, Lance</creatorcontrib><collection>American Chemical Society (ACS) Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Environmental science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fry, Juliane L</au><au>Draper, Danielle C</au><au>Barsanti, Kelley C</au><au>Smith, James N</au><au>Ortega, John</au><au>Winkler, Paul M</au><au>Lawler, Michael J</au><au>Brown, Steven S</au><au>Edwards, Peter M</au><au>Cohen, Ronald C</au><au>Lee, Lance</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Secondary Organic Aerosol Formation and Organic Nitrate Yield from NO3 Oxidation of Biogenic Hydrocarbons</atitle><jtitle>Environmental science & technology</jtitle><addtitle>Environ. Sci. Technol</addtitle><date>2014-10-21</date><risdate>2014</risdate><volume>48</volume><issue>20</issue><spage>11944</spage><epage>11953</epage><pages>11944-11953</pages><issn>0013-936X</issn><issn>1520-5851</issn><eissn>1520-5851</eissn><coden>ESTHAG</coden><abstract>The secondary organic aerosol (SOA) mass yields from NO3 oxidation of a series of biogenic volatile organic compounds (BVOCs), consisting of five monoterpenes and one sesquiterpene (α-pinene, β-pinene, Δ-3-carene, limonene, sabinene, and β-caryophyllene), were investigated in a series of continuous flow experiments in a 10 m3 indoor Teflon chamber. By making in situ measurements of the nitrate radical and employing a kinetics box model, we generate time-dependent yield curves as a function of reacted BVOC. SOA yields varied dramatically among the different BVOCs, from zero for α-pinene to 38–65% for Δ-3-carene and 86% for β-caryophyllene at mass loading of 10 μg m–3, suggesting that model mechanisms that treat all NO3 + monoterpene reactions equally will lead to errors in predicted SOA depending on each location’s mix of BVOC emissions. In most cases, organonitrate is a dominant component of the aerosol produced, but in the case of α-pinene, little organonitrate and no aerosol is formed.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>25229208</pmid><doi>10.1021/es502204x</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | aerosols Aerosols - chemistry Air Pollutants - analysis Air Pollutants - chemistry alpha-pinene Applied sciences Atmospheric pollution beta-caryophyllene beta-pinene Bridged Bicyclo Compounds - chemistry carene Cyclohexenes - chemistry Earth, ocean, space emissions Exact sciences and technology External geophysics Kinetics Limonene Meteorology Monoterpenes - chemistry nitrates Nitrates - chemistry oxidation Particles and aerosols Pollutants physicochemistry study: properties, effects, reactions, transport and distribution Pollution polytetrafluoroethylene sabinene Sesquiterpenes - chemistry Terpenes - chemistry volatile organic compounds Volatile Organic Compounds - chemistry |
title | Secondary Organic Aerosol Formation and Organic Nitrate Yield from NO3 Oxidation of Biogenic Hydrocarbons |
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