Atmospheric Mercury in the Barnett Shale Area, Texas: Implications for Emissions from Oil and Gas Processing
Atmospheric mercury emissions in the Barnett Shale area were studied by employing both stationary measurements and mobile laboratory surveys. Stationary measurements near the Engle Mountain Lake showed that the median mixing ratio of total gaseous mercury (THg) was 138 ppqv (140 ± 29 ppqv for mean ±...
Gespeichert in:
Veröffentlicht in: | Environmental science & technology 2015-09, Vol.49 (17), p.10692-10700 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 10700 |
---|---|
container_issue | 17 |
container_start_page | 10692 |
container_title | Environmental science & technology |
container_volume | 49 |
creator | Lan, Xin Talbot, Robert Laine, Patrick Torres, Azucena Lefer, Barry Flynn, James |
description | Atmospheric mercury emissions in the Barnett Shale area were studied by employing both stationary measurements and mobile laboratory surveys. Stationary measurements near the Engle Mountain Lake showed that the median mixing ratio of total gaseous mercury (THg) was 138 ppqv (140 ± 29 ppqv for mean ± S.D.) during the June 2011 study period. A distinct diurnal variation pattern was observed in which the highest THg levels appeared near midnight, followed by a monotonic decrease until midafternoon. The influence of oil and gas (ONG) emissions was substantial in this area, as inferred from the i-pentane/n-pentane ratio (1.17). However, few THg plumes were captured by our mobile laboratory during a ∼3700 km survey with detailed downwind measurements from 50 ONG facilities. One compressor station and one natural gas condensate processing facility were found to have significant THg emissions, with maximum THg levels of 963 and 392 ppqv, respectively, and the emissions rates were estimated to be 7.9 kg/yr and 0.3 kg/yr, respectively. Our results suggest that the majority of ONG facilities in this area are not significant sources of THg; however, it is highly likely that a small number of these facilities contribute a relatively large amount of emissions in the ONG sector. |
doi_str_mv | 10.1021/acs.est.5b02287 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1722168151</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1708902266</sourcerecordid><originalsourceid>FETCH-LOGICAL-a394t-bf53544dc1fe7043ce431ea8ca42625619dabeefdcf12ae6ff387f97bb0f5b973</originalsourceid><addsrcrecordid>eNqNkc1r3DAQxUVpaLZpz70VQS-BxpsZybLl3jYhX5CSQlPozcjyqOtgW1vJhua_r5bdNlAI9DSI-b03o3mMvUNYIgg8NTYuKU5L1YAQunzBFqgEZEorfMkWACizShbfD9nrGB8AQEjQr9ihKATq1FywfjUNPm7WFDrLP1Owc3jk3cinNfEzE0aaJv51bXriq0DmhN_TLxM_8Zth03fWTJ0fI3c-8Iuhi3H3Cn7gd13PzdjyKxP5l-Atpeb44w07cKaP9HZfj9i3y4v78-vs9u7q5nx1mxlZ5VPWOCVVnrcWHZWQS0u5RDLamjwtrgqsWtMQudY6FIYK56QuXVU2DTjVVKU8Ysc7303wP-d0nzptZ6nvzUh-jjWWQmChUeF_oKCrdNuiSOiHf9AHP4cxfSRRCCCFFpCo0x1lg48xkKs3oRtMeKwR6m1mdcqs3qr3mSXF-73v3AzU_uX_hJSAjztgq3ya-Yzdb8_ioaI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1710032820</pqid></control><display><type>article</type><title>Atmospheric Mercury in the Barnett Shale Area, Texas: Implications for Emissions from Oil and Gas Processing</title><source>MEDLINE</source><source>American Chemical Society Journals</source><creator>Lan, Xin ; Talbot, Robert ; Laine, Patrick ; Torres, Azucena ; Lefer, Barry ; Flynn, James</creator><creatorcontrib>Lan, Xin ; Talbot, Robert ; Laine, Patrick ; Torres, Azucena ; Lefer, Barry ; Flynn, James</creatorcontrib><description>Atmospheric mercury emissions in the Barnett Shale area were studied by employing both stationary measurements and mobile laboratory surveys. Stationary measurements near the Engle Mountain Lake showed that the median mixing ratio of total gaseous mercury (THg) was 138 ppqv (140 ± 29 ppqv for mean ± S.D.) during the June 2011 study period. A distinct diurnal variation pattern was observed in which the highest THg levels appeared near midnight, followed by a monotonic decrease until midafternoon. The influence of oil and gas (ONG) emissions was substantial in this area, as inferred from the i-pentane/n-pentane ratio (1.17). However, few THg plumes were captured by our mobile laboratory during a ∼3700 km survey with detailed downwind measurements from 50 ONG facilities. One compressor station and one natural gas condensate processing facility were found to have significant THg emissions, with maximum THg levels of 963 and 392 ppqv, respectively, and the emissions rates were estimated to be 7.9 kg/yr and 0.3 kg/yr, respectively. Our results suggest that the majority of ONG facilities in this area are not significant sources of THg; however, it is highly likely that a small number of these facilities contribute a relatively large amount of emissions in the ONG sector.</description><identifier>ISSN: 0013-936X</identifier><identifier>EISSN: 1520-5851</identifier><identifier>DOI: 10.1021/acs.est.5b02287</identifier><identifier>PMID: 26218013</identifier><identifier>CODEN: ESTHAG</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Air Pollutants - analysis ; Atmosphere - chemistry ; Carbon Monoxide - analysis ; Computer Simulation ; Emissions ; Geography ; Geologic Sediments - chemistry ; Laboratories ; Mercury ; Mercury - analysis ; Natural gas ; Natural Gas - analysis ; Oil and Gas Fields ; Sulfur Dioxide - analysis ; Texas ; Time Factors ; Volatile Organic Compounds - analysis</subject><ispartof>Environmental science & technology, 2015-09, Vol.49 (17), p.10692-10700</ispartof><rights>Copyright © American Chemical Society</rights><rights>Copyright American Chemical Society Sep 1, 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a394t-bf53544dc1fe7043ce431ea8ca42625619dabeefdcf12ae6ff387f97bb0f5b973</citedby><cites>FETCH-LOGICAL-a394t-bf53544dc1fe7043ce431ea8ca42625619dabeefdcf12ae6ff387f97bb0f5b973</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/acs.est.5b02287$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.est.5b02287$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26218013$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lan, Xin</creatorcontrib><creatorcontrib>Talbot, Robert</creatorcontrib><creatorcontrib>Laine, Patrick</creatorcontrib><creatorcontrib>Torres, Azucena</creatorcontrib><creatorcontrib>Lefer, Barry</creatorcontrib><creatorcontrib>Flynn, James</creatorcontrib><title>Atmospheric Mercury in the Barnett Shale Area, Texas: Implications for Emissions from Oil and Gas Processing</title><title>Environmental science & technology</title><addtitle>Environ. Sci. Technol</addtitle><description>Atmospheric mercury emissions in the Barnett Shale area were studied by employing both stationary measurements and mobile laboratory surveys. Stationary measurements near the Engle Mountain Lake showed that the median mixing ratio of total gaseous mercury (THg) was 138 ppqv (140 ± 29 ppqv for mean ± S.D.) during the June 2011 study period. A distinct diurnal variation pattern was observed in which the highest THg levels appeared near midnight, followed by a monotonic decrease until midafternoon. The influence of oil and gas (ONG) emissions was substantial in this area, as inferred from the i-pentane/n-pentane ratio (1.17). However, few THg plumes were captured by our mobile laboratory during a ∼3700 km survey with detailed downwind measurements from 50 ONG facilities. One compressor station and one natural gas condensate processing facility were found to have significant THg emissions, with maximum THg levels of 963 and 392 ppqv, respectively, and the emissions rates were estimated to be 7.9 kg/yr and 0.3 kg/yr, respectively. Our results suggest that the majority of ONG facilities in this area are not significant sources of THg; however, it is highly likely that a small number of these facilities contribute a relatively large amount of emissions in the ONG sector.</description><subject>Air Pollutants - analysis</subject><subject>Atmosphere - chemistry</subject><subject>Carbon Monoxide - analysis</subject><subject>Computer Simulation</subject><subject>Emissions</subject><subject>Geography</subject><subject>Geologic Sediments - chemistry</subject><subject>Laboratories</subject><subject>Mercury</subject><subject>Mercury - analysis</subject><subject>Natural gas</subject><subject>Natural Gas - analysis</subject><subject>Oil and Gas Fields</subject><subject>Sulfur Dioxide - analysis</subject><subject>Texas</subject><subject>Time Factors</subject><subject>Volatile Organic Compounds - analysis</subject><issn>0013-936X</issn><issn>1520-5851</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1r3DAQxUVpaLZpz70VQS-BxpsZybLl3jYhX5CSQlPozcjyqOtgW1vJhua_r5bdNlAI9DSI-b03o3mMvUNYIgg8NTYuKU5L1YAQunzBFqgEZEorfMkWACizShbfD9nrGB8AQEjQr9ihKATq1FywfjUNPm7WFDrLP1Owc3jk3cinNfEzE0aaJv51bXriq0DmhN_TLxM_8Zth03fWTJ0fI3c-8Iuhi3H3Cn7gd13PzdjyKxP5l-Atpeb44w07cKaP9HZfj9i3y4v78-vs9u7q5nx1mxlZ5VPWOCVVnrcWHZWQS0u5RDLamjwtrgqsWtMQudY6FIYK56QuXVU2DTjVVKU8Ysc7303wP-d0nzptZ6nvzUh-jjWWQmChUeF_oKCrdNuiSOiHf9AHP4cxfSRRCCCFFpCo0x1lg48xkKs3oRtMeKwR6m1mdcqs3qr3mSXF-73v3AzU_uX_hJSAjztgq3ya-Yzdb8_ioaI</recordid><startdate>20150901</startdate><enddate>20150901</enddate><creator>Lan, Xin</creator><creator>Talbot, Robert</creator><creator>Laine, Patrick</creator><creator>Torres, Azucena</creator><creator>Lefer, Barry</creator><creator>Flynn, James</creator><general>American Chemical Society</general><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><scope>7X8</scope><scope>7QH</scope><scope>7TG</scope><scope>7TV</scope><scope>7UA</scope><scope>F1W</scope><scope>H97</scope><scope>KL.</scope><scope>L.G</scope></search><sort><creationdate>20150901</creationdate><title>Atmospheric Mercury in the Barnett Shale Area, Texas: Implications for Emissions from Oil and Gas Processing</title><author>Lan, Xin ; Talbot, Robert ; Laine, Patrick ; Torres, Azucena ; Lefer, Barry ; Flynn, James</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a394t-bf53544dc1fe7043ce431ea8ca42625619dabeefdcf12ae6ff387f97bb0f5b973</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Air Pollutants - analysis</topic><topic>Atmosphere - chemistry</topic><topic>Carbon Monoxide - analysis</topic><topic>Computer Simulation</topic><topic>Emissions</topic><topic>Geography</topic><topic>Geologic Sediments - chemistry</topic><topic>Laboratories</topic><topic>Mercury</topic><topic>Mercury - analysis</topic><topic>Natural gas</topic><topic>Natural Gas - analysis</topic><topic>Oil and Gas Fields</topic><topic>Sulfur Dioxide - analysis</topic><topic>Texas</topic><topic>Time Factors</topic><topic>Volatile Organic Compounds - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lan, Xin</creatorcontrib><creatorcontrib>Talbot, Robert</creatorcontrib><creatorcontrib>Laine, Patrick</creatorcontrib><creatorcontrib>Torres, Azucena</creatorcontrib><creatorcontrib>Lefer, Barry</creatorcontrib><creatorcontrib>Flynn, James</creatorcontrib><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><collection>MEDLINE - Academic</collection><collection>Aqualine</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Pollution Abstracts</collection><collection>Water Resources Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><jtitle>Environmental science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lan, Xin</au><au>Talbot, Robert</au><au>Laine, Patrick</au><au>Torres, Azucena</au><au>Lefer, Barry</au><au>Flynn, James</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Atmospheric Mercury in the Barnett Shale Area, Texas: Implications for Emissions from Oil and Gas Processing</atitle><jtitle>Environmental science & technology</jtitle><addtitle>Environ. Sci. Technol</addtitle><date>2015-09-01</date><risdate>2015</risdate><volume>49</volume><issue>17</issue><spage>10692</spage><epage>10700</epage><pages>10692-10700</pages><issn>0013-936X</issn><eissn>1520-5851</eissn><coden>ESTHAG</coden><abstract>Atmospheric mercury emissions in the Barnett Shale area were studied by employing both stationary measurements and mobile laboratory surveys. Stationary measurements near the Engle Mountain Lake showed that the median mixing ratio of total gaseous mercury (THg) was 138 ppqv (140 ± 29 ppqv for mean ± S.D.) during the June 2011 study period. A distinct diurnal variation pattern was observed in which the highest THg levels appeared near midnight, followed by a monotonic decrease until midafternoon. The influence of oil and gas (ONG) emissions was substantial in this area, as inferred from the i-pentane/n-pentane ratio (1.17). However, few THg plumes were captured by our mobile laboratory during a ∼3700 km survey with detailed downwind measurements from 50 ONG facilities. One compressor station and one natural gas condensate processing facility were found to have significant THg emissions, with maximum THg levels of 963 and 392 ppqv, respectively, and the emissions rates were estimated to be 7.9 kg/yr and 0.3 kg/yr, respectively. Our results suggest that the majority of ONG facilities in this area are not significant sources of THg; however, it is highly likely that a small number of these facilities contribute a relatively large amount of emissions in the ONG sector.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>26218013</pmid><doi>10.1021/acs.est.5b02287</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0013-936X |
ispartof | Environmental science & technology, 2015-09, Vol.49 (17), p.10692-10700 |
issn | 0013-936X 1520-5851 |
language | eng |
recordid | cdi_proquest_miscellaneous_1722168151 |
source | MEDLINE; American Chemical Society Journals |
subjects | Air Pollutants - analysis Atmosphere - chemistry Carbon Monoxide - analysis Computer Simulation Emissions Geography Geologic Sediments - chemistry Laboratories Mercury Mercury - analysis Natural gas Natural Gas - analysis Oil and Gas Fields Sulfur Dioxide - analysis Texas Time Factors Volatile Organic Compounds - analysis |
title | Atmospheric Mercury in the Barnett Shale Area, Texas: Implications for Emissions from Oil and Gas Processing |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T06%3A27%3A17IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Atmospheric%20Mercury%20in%20the%20Barnett%20Shale%20Area,%20Texas:%20Implications%20for%20Emissions%20from%20Oil%20and%20Gas%20Processing&rft.jtitle=Environmental%20science%20&%20technology&rft.au=Lan,%20Xin&rft.date=2015-09-01&rft.volume=49&rft.issue=17&rft.spage=10692&rft.epage=10700&rft.pages=10692-10700&rft.issn=0013-936X&rft.eissn=1520-5851&rft.coden=ESTHAG&rft_id=info:doi/10.1021/acs.est.5b02287&rft_dat=%3Cproquest_cross%3E1708902266%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1710032820&rft_id=info:pmid/26218013&rfr_iscdi=true |