Equivalence of Elemental Carbon by Thermal/Optical Reflectance and Transmittance with Different Temperature Protocols
Charring of organic carbon (OC) during thermal/optical analysis is monitored by the change in a laser signal either reflected from or transmitted through a filter punch. Elemental carbon (EC) in suspended particulate matter collected on quartz-fiber filters is defined as the carbon that evolves afte...
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description | Charring of organic carbon (OC) during thermal/optical analysis is monitored by the change in a laser signal either reflected from or transmitted through a filter punch. Elemental carbon (EC) in suspended particulate matter collected on quartz-fiber filters is defined as the carbon that evolves after the detected optical signal attains the value it had prior to commencement of heating, with the rest of the carbon classified as organic carbon (OC). Heretofore, operational definitions of EC were believed to be caused by different temperature protocols rather than by the method of monitoring charring. This work demonstrates that thermal/optical reflectance (TOR) corrections yield equivalent OC/EC splits for widely divergent temperature protocols. EC results determined by simultaneous thermal/optical transmittance (TOT) corrections are 30% lower than TOR for the same temperature protocol and 70−80% lower than TOR for a protocol with higher heating temperatures and shorter residence times. This is true for 58 urban samples from Fresno, CA, as well as for 30 samples from the nonurban IMPROVE network that are individually dominated by wildfire, vehicle exhaust, secondary organic aerosol, and calcium carbonate contributions. Visual examination of filter darkening at different temperature stages shows that substantial charring takes place within the filter, possibly due to adsorbed organic gases or diffusion of vaporized particles. The filter transmittance is more influenced by the within-filter char, whereas the filter reflectance is dominated by charring of the near-surface deposit that appears to evolve first when oxygen is added to helium in the analysis atmosphere for these samples. The amounts of charred OC (POC) and EC are also estimated from incremental absorbance. Small amounts of POC are found to dominate the incremental absorbance. EC estimated from absorbance are found to agree better with EC from the reflectance charring correction than with EC from the transmittance charring correction. |
doi_str_mv | 10.1021/es034936u |
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Antony ; Arnott, W. Patrick ; Moosmüller, Hans ; Fung, Kochy</creator><creatorcontrib>Chow, Judith C ; Watson, John G ; Chen, L.-W. Antony ; Arnott, W. Patrick ; Moosmüller, Hans ; Fung, Kochy</creatorcontrib><description>Charring of organic carbon (OC) during thermal/optical analysis is monitored by the change in a laser signal either reflected from or transmitted through a filter punch. Elemental carbon (EC) in suspended particulate matter collected on quartz-fiber filters is defined as the carbon that evolves after the detected optical signal attains the value it had prior to commencement of heating, with the rest of the carbon classified as organic carbon (OC). Heretofore, operational definitions of EC were believed to be caused by different temperature protocols rather than by the method of monitoring charring. This work demonstrates that thermal/optical reflectance (TOR) corrections yield equivalent OC/EC splits for widely divergent temperature protocols. EC results determined by simultaneous thermal/optical transmittance (TOT) corrections are 30% lower than TOR for the same temperature protocol and 70−80% lower than TOR for a protocol with higher heating temperatures and shorter residence times. This is true for 58 urban samples from Fresno, CA, as well as for 30 samples from the nonurban IMPROVE network that are individually dominated by wildfire, vehicle exhaust, secondary organic aerosol, and calcium carbonate contributions. Visual examination of filter darkening at different temperature stages shows that substantial charring takes place within the filter, possibly due to adsorbed organic gases or diffusion of vaporized particles. The filter transmittance is more influenced by the within-filter char, whereas the filter reflectance is dominated by charring of the near-surface deposit that appears to evolve first when oxygen is added to helium in the analysis atmosphere for these samples. The amounts of charred OC (POC) and EC are also estimated from incremental absorbance. Small amounts of POC are found to dominate the incremental absorbance. EC estimated from absorbance are found to agree better with EC from the reflectance charring correction than with EC from the transmittance charring correction.</description><identifier>ISSN: 0013-936X</identifier><identifier>EISSN: 1520-5851</identifier><identifier>DOI: 10.1021/es034936u</identifier><identifier>PMID: 15382872</identifier><identifier>CODEN: ESTHAG</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Adsorption ; Applied sciences ; Atmospheric pollution ; Carbon ; Carbon - chemistry ; Earth, ocean, space ; Environmental Monitoring - methods ; Exact sciences and technology ; External geophysics ; Filters ; Filtration ; Meteorology ; Optics and Photonics ; Particles and aerosols ; Pollutants physicochemistry study: properties, effects, reactions, transport and distribution ; Pollution ; Temperature ; Temperature effects</subject><ispartof>Environmental science & technology, 2004-08, Vol.38 (16), p.4414-4422</ispartof><rights>Copyright © 2004 American Chemical Society</rights><rights>2004 INIST-CNRS</rights><rights>Copyright American Chemical Society Aug 15, 2004</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a406t-cd901617715211eaa3b931e2ca88690c734a80370ca3b4f9db4886468d9434c13</citedby><cites>FETCH-LOGICAL-a406t-cd901617715211eaa3b931e2ca88690c734a80370ca3b4f9db4886468d9434c13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/es034936u$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/es034936u$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16025406$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15382872$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chow, Judith C</creatorcontrib><creatorcontrib>Watson, John G</creatorcontrib><creatorcontrib>Chen, L.-W. Antony</creatorcontrib><creatorcontrib>Arnott, W. Patrick</creatorcontrib><creatorcontrib>Moosmüller, Hans</creatorcontrib><creatorcontrib>Fung, Kochy</creatorcontrib><title>Equivalence of Elemental Carbon by Thermal/Optical Reflectance and Transmittance with Different Temperature Protocols</title><title>Environmental science & technology</title><addtitle>Environ. Sci. Technol</addtitle><description>Charring of organic carbon (OC) during thermal/optical analysis is monitored by the change in a laser signal either reflected from or transmitted through a filter punch. Elemental carbon (EC) in suspended particulate matter collected on quartz-fiber filters is defined as the carbon that evolves after the detected optical signal attains the value it had prior to commencement of heating, with the rest of the carbon classified as organic carbon (OC). Heretofore, operational definitions of EC were believed to be caused by different temperature protocols rather than by the method of monitoring charring. This work demonstrates that thermal/optical reflectance (TOR) corrections yield equivalent OC/EC splits for widely divergent temperature protocols. EC results determined by simultaneous thermal/optical transmittance (TOT) corrections are 30% lower than TOR for the same temperature protocol and 70−80% lower than TOR for a protocol with higher heating temperatures and shorter residence times. This is true for 58 urban samples from Fresno, CA, as well as for 30 samples from the nonurban IMPROVE network that are individually dominated by wildfire, vehicle exhaust, secondary organic aerosol, and calcium carbonate contributions. Visual examination of filter darkening at different temperature stages shows that substantial charring takes place within the filter, possibly due to adsorbed organic gases or diffusion of vaporized particles. The filter transmittance is more influenced by the within-filter char, whereas the filter reflectance is dominated by charring of the near-surface deposit that appears to evolve first when oxygen is added to helium in the analysis atmosphere for these samples. The amounts of charred OC (POC) and EC are also estimated from incremental absorbance. Small amounts of POC are found to dominate the incremental absorbance. EC estimated from absorbance are found to agree better with EC from the reflectance charring correction than with EC from the transmittance charring correction.</description><subject>Adsorption</subject><subject>Applied sciences</subject><subject>Atmospheric pollution</subject><subject>Carbon</subject><subject>Carbon - chemistry</subject><subject>Earth, ocean, space</subject><subject>Environmental Monitoring - methods</subject><subject>Exact sciences and technology</subject><subject>External geophysics</subject><subject>Filters</subject><subject>Filtration</subject><subject>Meteorology</subject><subject>Optics and Photonics</subject><subject>Particles and aerosols</subject><subject>Pollutants physicochemistry study: properties, effects, reactions, transport and distribution</subject><subject>Pollution</subject><subject>Temperature</subject><subject>Temperature effects</subject><issn>0013-936X</issn><issn>1520-5851</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNplkE1v1DAQhi0EotvCgT-ALCQOPYSO43zYRxSW0mqlViVIiIs1cSZqSj62tgP03-NqV91DT5bmffza8zD2TsAnAak4Iw8y07JYXrCVyFNIcpWLl2wFIGQS5z-P2LH3dwCQSlCv2ZHIpUpVma7Ysr5f-j840GSJzx1fDzTSFHDgFbpmnnjzwOtbciMOZ1fb0NuY3FA3kA34eAWnltcOJz_2YTf524db_qXvOnKxiNc0bslhWBzxazeH2c6Df8NedTh4ers_T9iPr-u6-pZsrs4vqs-bBDMoQmJbDaIQZRmXEoIQZaOloNSiUoUGW8oMFcgSbEyyTrdNFoOsUK3OZGaFPGEfdr1bN98v5IO5mxc3xSdNNCFSraWK0OkOsm723lFntq4f0T0YAebRr3nyG9n3-8KlGak9kHuhEfi4B9BHV11UY3t_4ApI87hb5JId1_tA_55ydL9NUcoyN_X1d3NZ6WoD-bn5dehF6w9LPP_gf3pAndM</recordid><startdate>20040815</startdate><enddate>20040815</enddate><creator>Chow, Judith C</creator><creator>Watson, John G</creator><creator>Chen, L.-W. Antony</creator><creator>Arnott, W. Patrick</creator><creator>Moosmüller, Hans</creator><creator>Fung, Kochy</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7ST</scope><scope>7T7</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>SOI</scope></search><sort><creationdate>20040815</creationdate><title>Equivalence of Elemental Carbon by Thermal/Optical Reflectance and Transmittance with Different Temperature Protocols</title><author>Chow, Judith C ; Watson, John G ; Chen, L.-W. Antony ; Arnott, W. Patrick ; Moosmüller, Hans ; Fung, Kochy</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a406t-cd901617715211eaa3b931e2ca88690c734a80370ca3b4f9db4886468d9434c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adsorption</topic><topic>Applied sciences</topic><topic>Atmospheric pollution</topic><topic>Carbon</topic><topic>Carbon - chemistry</topic><topic>Earth, ocean, space</topic><topic>Environmental Monitoring - methods</topic><topic>Exact sciences and technology</topic><topic>External geophysics</topic><topic>Filters</topic><topic>Filtration</topic><topic>Meteorology</topic><topic>Optics and Photonics</topic><topic>Particles and aerosols</topic><topic>Pollutants physicochemistry study: properties, effects, reactions, transport and distribution</topic><topic>Pollution</topic><topic>Temperature</topic><topic>Temperature effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chow, Judith C</creatorcontrib><creatorcontrib>Watson, John G</creatorcontrib><creatorcontrib>Chen, L.-W. Antony</creatorcontrib><creatorcontrib>Arnott, W. Patrick</creatorcontrib><creatorcontrib>Moosmüller, Hans</creatorcontrib><creatorcontrib>Fung, Kochy</creatorcontrib><collection>Istex</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>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><jtitle>Environmental science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chow, Judith C</au><au>Watson, John G</au><au>Chen, L.-W. Antony</au><au>Arnott, W. Patrick</au><au>Moosmüller, Hans</au><au>Fung, Kochy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Equivalence of Elemental Carbon by Thermal/Optical Reflectance and Transmittance with Different Temperature Protocols</atitle><jtitle>Environmental science & technology</jtitle><addtitle>Environ. Sci. Technol</addtitle><date>2004-08-15</date><risdate>2004</risdate><volume>38</volume><issue>16</issue><spage>4414</spage><epage>4422</epage><pages>4414-4422</pages><issn>0013-936X</issn><eissn>1520-5851</eissn><coden>ESTHAG</coden><abstract>Charring of organic carbon (OC) during thermal/optical analysis is monitored by the change in a laser signal either reflected from or transmitted through a filter punch. Elemental carbon (EC) in suspended particulate matter collected on quartz-fiber filters is defined as the carbon that evolves after the detected optical signal attains the value it had prior to commencement of heating, with the rest of the carbon classified as organic carbon (OC). Heretofore, operational definitions of EC were believed to be caused by different temperature protocols rather than by the method of monitoring charring. This work demonstrates that thermal/optical reflectance (TOR) corrections yield equivalent OC/EC splits for widely divergent temperature protocols. EC results determined by simultaneous thermal/optical transmittance (TOT) corrections are 30% lower than TOR for the same temperature protocol and 70−80% lower than TOR for a protocol with higher heating temperatures and shorter residence times. This is true for 58 urban samples from Fresno, CA, as well as for 30 samples from the nonurban IMPROVE network that are individually dominated by wildfire, vehicle exhaust, secondary organic aerosol, and calcium carbonate contributions. Visual examination of filter darkening at different temperature stages shows that substantial charring takes place within the filter, possibly due to adsorbed organic gases or diffusion of vaporized particles. The filter transmittance is more influenced by the within-filter char, whereas the filter reflectance is dominated by charring of the near-surface deposit that appears to evolve first when oxygen is added to helium in the analysis atmosphere for these samples. The amounts of charred OC (POC) and EC are also estimated from incremental absorbance. Small amounts of POC are found to dominate the incremental absorbance. EC estimated from absorbance are found to agree better with EC from the reflectance charring correction than with EC from the transmittance charring correction.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>15382872</pmid><doi>10.1021/es034936u</doi><tpages>9</tpages></addata></record> |
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subjects | Adsorption Applied sciences Atmospheric pollution Carbon Carbon - chemistry Earth, ocean, space Environmental Monitoring - methods Exact sciences and technology External geophysics Filters Filtration Meteorology Optics and Photonics Particles and aerosols Pollutants physicochemistry study: properties, effects, reactions, transport and distribution Pollution Temperature Temperature effects |
title | Equivalence of Elemental Carbon by Thermal/Optical Reflectance and Transmittance with Different Temperature Protocols |
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