Intense secondary aerosol formation due to strong atmospheric photochemical reactions in summer: observations at a rural site in eastern Yangtze River Delta of China

High pollution episodes of PM2.5 and O3 were frequently observed at a rural site (N31.0935º, E120.978°) in eastern Yangtze River Delta (YRD) in summer. To study the impacts of photochemical reactions on secondary aerosol formation in this region, we performed real-time measurements of the mass conce...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Science of the total environment 2016-11, Vol.571, p.1454-1466
Hauptverfasser: Wang, Dongfang, Zhou, Bin, Fu, Qingyan, Zhao, Qianbiao, Zhang, Qi, Chen, Jianmin, Yang, Xin, Duan, Yusen, Li, Juan
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1466
container_issue
container_start_page 1454
container_title The Science of the total environment
container_volume 571
creator Wang, Dongfang
Zhou, Bin
Fu, Qingyan
Zhao, Qianbiao
Zhang, Qi
Chen, Jianmin
Yang, Xin
Duan, Yusen
Li, Juan
description High pollution episodes of PM2.5 and O3 were frequently observed at a rural site (N31.0935º, E120.978°) in eastern Yangtze River Delta (YRD) in summer. To study the impacts of photochemical reactions on secondary aerosol formation in this region, we performed real-time measurements of the mass concentration and composition of PM2.5, particle size distribution (13.6~736.5 nm), concentrations of gas pollutants including O3, SO2, NO2, CO, non-methane hydrocarbons (NMHC)), and nitrate radical in 2013. During the sampling period, the average concentration of PM2.5 was 76.1 (± 16.5) μg/m3, in which secondary aerosol species including sulfate, nitrate, ammonium, and secondary organic aerosol (SOA) accounted for ~ 62%. Gas-phase oxidation of SO2 was mainly responsible for a fast increase of sulfate (at 1.70 μg/m3/h) in the morning. Photochemical production of nitric acid was intense during daytime, but particulate nitrate concentration was low in the afternoon due to high temperature. At night, nitrate was mainly formed through the hydrolysis of NO3 and/or N2O5. The correlations among NMHC, Ox (= O3 + NO2), and SOA suggested that a combination of high emission of hydrocarbons and active photochemical reactions led to the rapid formation of SOA. In addition, several new particle formation and fast growth events were observed despite high ambient aerosol loading. Since the onset of new particle events was accompanied by a rapid increase of H2SO4 and SOA, enhanced formation of sulfate and SOA driven by photochemical oxidation likely promoted the formation and growth of new particles. Together, our results demonstrated that strong atmospheric photochemical reactions enhanced secondary aerosols formation and led to the synchronous occurrence of high concentrations of PM2.5 and O3 in a regional scale. These findings are important for better understanding the air pollution in summer in YRD. [Display omitted] •High pollution episodes of both PM2.5 and O3 were observed in summer in YRD.•Formation mechanisms of secondary aerosol were studied by real-time measurement.•Secondary aerosol formation was enhanced by photochemical reactions.•New particle formation and growth was observed despite high aerosol loading.•Control measures for PM2.5 and O3 must be considered holistically in YRD.
doi_str_mv 10.1016/j.scitotenv.2016.06.212
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1827908173</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0048969716314012</els_id><sourcerecordid>1827908173</sourcerecordid><originalsourceid>FETCH-LOGICAL-c470t-48a909b98a57fee59400be9d3dd6b77de334655c32a92c7ef99a51ef5be784db3</originalsourceid><addsrcrecordid>eNqFkU1v1DAQhi1ERbeFvwBz5JJg58sxt2pLP6RKSAgOnCzHnnS9SuzFdlaC_8P_rKMtvTKXkUbP-45mXkI-MFoyyrpP-zJqm3xCdyyrPChpV1asekU2rOeiYLTqXpMNpU1fiE7wc3IR457m4j17Q84r3rC-ZXxD_t67bBIRImrvjAq_QWHw0U8w-jCrZL0DsyAkDzEF7x5BpdnHww6D1XDY-eT1Dmer1QQBlV4FEayDuMwzhs_gh4jhqE5zlUBBWEKGo024cqhiwuDgp3KP6Q_CN3vEANc4JQV-hO3OOvWWnI1qivjuuV-SHzdfvm_vioevt_fbq4dCN5ymoumVoGIQvWr5iNiKhtIBhamN6QbODdZ107WtrislKs1xFEK1DMd2QN43ZqgvyceT7yH4XwvGJGcbNU6TcuiXKFlfcUF7xuuM8hOq87diwFEegp3z_ySjcs1I7uVLRnLNSNJO5oyy8v3zkmWY0bzo_oWSgasTgPnUo8WwGqHTaGxAnaTx9r9LngDjmqxE</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1827908173</pqid></control><display><type>article</type><title>Intense secondary aerosol formation due to strong atmospheric photochemical reactions in summer: observations at a rural site in eastern Yangtze River Delta of China</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Wang, Dongfang ; Zhou, Bin ; Fu, Qingyan ; Zhao, Qianbiao ; Zhang, Qi ; Chen, Jianmin ; Yang, Xin ; Duan, Yusen ; Li, Juan</creator><creatorcontrib>Wang, Dongfang ; Zhou, Bin ; Fu, Qingyan ; Zhao, Qianbiao ; Zhang, Qi ; Chen, Jianmin ; Yang, Xin ; Duan, Yusen ; Li, Juan</creatorcontrib><description>High pollution episodes of PM2.5 and O3 were frequently observed at a rural site (N31.0935º, E120.978°) in eastern Yangtze River Delta (YRD) in summer. To study the impacts of photochemical reactions on secondary aerosol formation in this region, we performed real-time measurements of the mass concentration and composition of PM2.5, particle size distribution (13.6~736.5 nm), concentrations of gas pollutants including O3, SO2, NO2, CO, non-methane hydrocarbons (NMHC)), and nitrate radical in 2013. During the sampling period, the average concentration of PM2.5 was 76.1 (± 16.5) μg/m3, in which secondary aerosol species including sulfate, nitrate, ammonium, and secondary organic aerosol (SOA) accounted for ~ 62%. Gas-phase oxidation of SO2 was mainly responsible for a fast increase of sulfate (at 1.70 μg/m3/h) in the morning. Photochemical production of nitric acid was intense during daytime, but particulate nitrate concentration was low in the afternoon due to high temperature. At night, nitrate was mainly formed through the hydrolysis of NO3 and/or N2O5. The correlations among NMHC, Ox (= O3 + NO2), and SOA suggested that a combination of high emission of hydrocarbons and active photochemical reactions led to the rapid formation of SOA. In addition, several new particle formation and fast growth events were observed despite high ambient aerosol loading. Since the onset of new particle events was accompanied by a rapid increase of H2SO4 and SOA, enhanced formation of sulfate and SOA driven by photochemical oxidation likely promoted the formation and growth of new particles. Together, our results demonstrated that strong atmospheric photochemical reactions enhanced secondary aerosols formation and led to the synchronous occurrence of high concentrations of PM2.5 and O3 in a regional scale. These findings are important for better understanding the air pollution in summer in YRD. [Display omitted] •High pollution episodes of both PM2.5 and O3 were observed in summer in YRD.•Formation mechanisms of secondary aerosol were studied by real-time measurement.•Secondary aerosol formation was enhanced by photochemical reactions.•New particle formation and growth was observed despite high aerosol loading.•Control measures for PM2.5 and O3 must be considered holistically in YRD.</description><identifier>ISSN: 0048-9697</identifier><identifier>EISSN: 1879-1026</identifier><identifier>DOI: 10.1016/j.scitotenv.2016.06.212</identifier><identifier>PMID: 27418517</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Aerosols - analysis ; Air Pollutants - analysis ; China ; Environmental Monitoring ; Gaseous Precursors ; Ozone - analysis ; Particle Size ; Particulate Matter - analysis ; Photochemical Oxidation ; Photochemical Processes ; PM2.5 ; Seasons ; Secondary Aerosol Formation ; Yangtze River Delta</subject><ispartof>The Science of the total environment, 2016-11, Vol.571, p.1454-1466</ispartof><rights>2016 Elsevier B.V.</rights><rights>Copyright © 2016 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-48a909b98a57fee59400be9d3dd6b77de334655c32a92c7ef99a51ef5be784db3</citedby><cites>FETCH-LOGICAL-c470t-48a909b98a57fee59400be9d3dd6b77de334655c32a92c7ef99a51ef5be784db3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0048969716314012$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27418517$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Dongfang</creatorcontrib><creatorcontrib>Zhou, Bin</creatorcontrib><creatorcontrib>Fu, Qingyan</creatorcontrib><creatorcontrib>Zhao, Qianbiao</creatorcontrib><creatorcontrib>Zhang, Qi</creatorcontrib><creatorcontrib>Chen, Jianmin</creatorcontrib><creatorcontrib>Yang, Xin</creatorcontrib><creatorcontrib>Duan, Yusen</creatorcontrib><creatorcontrib>Li, Juan</creatorcontrib><title>Intense secondary aerosol formation due to strong atmospheric photochemical reactions in summer: observations at a rural site in eastern Yangtze River Delta of China</title><title>The Science of the total environment</title><addtitle>Sci Total Environ</addtitle><description>High pollution episodes of PM2.5 and O3 were frequently observed at a rural site (N31.0935º, E120.978°) in eastern Yangtze River Delta (YRD) in summer. To study the impacts of photochemical reactions on secondary aerosol formation in this region, we performed real-time measurements of the mass concentration and composition of PM2.5, particle size distribution (13.6~736.5 nm), concentrations of gas pollutants including O3, SO2, NO2, CO, non-methane hydrocarbons (NMHC)), and nitrate radical in 2013. During the sampling period, the average concentration of PM2.5 was 76.1 (± 16.5) μg/m3, in which secondary aerosol species including sulfate, nitrate, ammonium, and secondary organic aerosol (SOA) accounted for ~ 62%. Gas-phase oxidation of SO2 was mainly responsible for a fast increase of sulfate (at 1.70 μg/m3/h) in the morning. Photochemical production of nitric acid was intense during daytime, but particulate nitrate concentration was low in the afternoon due to high temperature. At night, nitrate was mainly formed through the hydrolysis of NO3 and/or N2O5. The correlations among NMHC, Ox (= O3 + NO2), and SOA suggested that a combination of high emission of hydrocarbons and active photochemical reactions led to the rapid formation of SOA. In addition, several new particle formation and fast growth events were observed despite high ambient aerosol loading. Since the onset of new particle events was accompanied by a rapid increase of H2SO4 and SOA, enhanced formation of sulfate and SOA driven by photochemical oxidation likely promoted the formation and growth of new particles. Together, our results demonstrated that strong atmospheric photochemical reactions enhanced secondary aerosols formation and led to the synchronous occurrence of high concentrations of PM2.5 and O3 in a regional scale. These findings are important for better understanding the air pollution in summer in YRD. [Display omitted] •High pollution episodes of both PM2.5 and O3 were observed in summer in YRD.•Formation mechanisms of secondary aerosol were studied by real-time measurement.•Secondary aerosol formation was enhanced by photochemical reactions.•New particle formation and growth was observed despite high aerosol loading.•Control measures for PM2.5 and O3 must be considered holistically in YRD.</description><subject>Aerosols - analysis</subject><subject>Air Pollutants - analysis</subject><subject>China</subject><subject>Environmental Monitoring</subject><subject>Gaseous Precursors</subject><subject>Ozone - analysis</subject><subject>Particle Size</subject><subject>Particulate Matter - analysis</subject><subject>Photochemical Oxidation</subject><subject>Photochemical Processes</subject><subject>PM2.5</subject><subject>Seasons</subject><subject>Secondary Aerosol Formation</subject><subject>Yangtze River Delta</subject><issn>0048-9697</issn><issn>1879-1026</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi1ERbeFvwBz5JJg58sxt2pLP6RKSAgOnCzHnnS9SuzFdlaC_8P_rKMtvTKXkUbP-45mXkI-MFoyyrpP-zJqm3xCdyyrPChpV1asekU2rOeiYLTqXpMNpU1fiE7wc3IR457m4j17Q84r3rC-ZXxD_t67bBIRImrvjAq_QWHw0U8w-jCrZL0DsyAkDzEF7x5BpdnHww6D1XDY-eT1Dmer1QQBlV4FEayDuMwzhs_gh4jhqE5zlUBBWEKGo024cqhiwuDgp3KP6Q_CN3vEANc4JQV-hO3OOvWWnI1qivjuuV-SHzdfvm_vioevt_fbq4dCN5ymoumVoGIQvWr5iNiKhtIBhamN6QbODdZ107WtrislKs1xFEK1DMd2QN43ZqgvyceT7yH4XwvGJGcbNU6TcuiXKFlfcUF7xuuM8hOq87diwFEegp3z_ySjcs1I7uVLRnLNSNJO5oyy8v3zkmWY0bzo_oWSgasTgPnUo8WwGqHTaGxAnaTx9r9LngDjmqxE</recordid><startdate>20161115</startdate><enddate>20161115</enddate><creator>Wang, Dongfang</creator><creator>Zhou, Bin</creator><creator>Fu, Qingyan</creator><creator>Zhao, Qianbiao</creator><creator>Zhang, Qi</creator><creator>Chen, Jianmin</creator><creator>Yang, Xin</creator><creator>Duan, Yusen</creator><creator>Li, Juan</creator><general>Elsevier B.V</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>7ST</scope><scope>7TV</scope><scope>C1K</scope><scope>SOI</scope></search><sort><creationdate>20161115</creationdate><title>Intense secondary aerosol formation due to strong atmospheric photochemical reactions in summer: observations at a rural site in eastern Yangtze River Delta of China</title><author>Wang, Dongfang ; Zhou, Bin ; Fu, Qingyan ; Zhao, Qianbiao ; Zhang, Qi ; Chen, Jianmin ; Yang, Xin ; Duan, Yusen ; Li, Juan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-48a909b98a57fee59400be9d3dd6b77de334655c32a92c7ef99a51ef5be784db3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Aerosols - analysis</topic><topic>Air Pollutants - analysis</topic><topic>China</topic><topic>Environmental Monitoring</topic><topic>Gaseous Precursors</topic><topic>Ozone - analysis</topic><topic>Particle Size</topic><topic>Particulate Matter - analysis</topic><topic>Photochemical Oxidation</topic><topic>Photochemical Processes</topic><topic>PM2.5</topic><topic>Seasons</topic><topic>Secondary Aerosol Formation</topic><topic>Yangtze River Delta</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Dongfang</creatorcontrib><creatorcontrib>Zhou, Bin</creatorcontrib><creatorcontrib>Fu, Qingyan</creatorcontrib><creatorcontrib>Zhao, Qianbiao</creatorcontrib><creatorcontrib>Zhang, Qi</creatorcontrib><creatorcontrib>Chen, Jianmin</creatorcontrib><creatorcontrib>Yang, Xin</creatorcontrib><creatorcontrib>Duan, Yusen</creatorcontrib><creatorcontrib>Li, Juan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Pollution Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><jtitle>The Science of the total environment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Dongfang</au><au>Zhou, Bin</au><au>Fu, Qingyan</au><au>Zhao, Qianbiao</au><au>Zhang, Qi</au><au>Chen, Jianmin</au><au>Yang, Xin</au><au>Duan, Yusen</au><au>Li, Juan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intense secondary aerosol formation due to strong atmospheric photochemical reactions in summer: observations at a rural site in eastern Yangtze River Delta of China</atitle><jtitle>The Science of the total environment</jtitle><addtitle>Sci Total Environ</addtitle><date>2016-11-15</date><risdate>2016</risdate><volume>571</volume><spage>1454</spage><epage>1466</epage><pages>1454-1466</pages><issn>0048-9697</issn><eissn>1879-1026</eissn><abstract>High pollution episodes of PM2.5 and O3 were frequently observed at a rural site (N31.0935º, E120.978°) in eastern Yangtze River Delta (YRD) in summer. To study the impacts of photochemical reactions on secondary aerosol formation in this region, we performed real-time measurements of the mass concentration and composition of PM2.5, particle size distribution (13.6~736.5 nm), concentrations of gas pollutants including O3, SO2, NO2, CO, non-methane hydrocarbons (NMHC)), and nitrate radical in 2013. During the sampling period, the average concentration of PM2.5 was 76.1 (± 16.5) μg/m3, in which secondary aerosol species including sulfate, nitrate, ammonium, and secondary organic aerosol (SOA) accounted for ~ 62%. Gas-phase oxidation of SO2 was mainly responsible for a fast increase of sulfate (at 1.70 μg/m3/h) in the morning. Photochemical production of nitric acid was intense during daytime, but particulate nitrate concentration was low in the afternoon due to high temperature. At night, nitrate was mainly formed through the hydrolysis of NO3 and/or N2O5. The correlations among NMHC, Ox (= O3 + NO2), and SOA suggested that a combination of high emission of hydrocarbons and active photochemical reactions led to the rapid formation of SOA. In addition, several new particle formation and fast growth events were observed despite high ambient aerosol loading. Since the onset of new particle events was accompanied by a rapid increase of H2SO4 and SOA, enhanced formation of sulfate and SOA driven by photochemical oxidation likely promoted the formation and growth of new particles. Together, our results demonstrated that strong atmospheric photochemical reactions enhanced secondary aerosols formation and led to the synchronous occurrence of high concentrations of PM2.5 and O3 in a regional scale. These findings are important for better understanding the air pollution in summer in YRD. [Display omitted] •High pollution episodes of both PM2.5 and O3 were observed in summer in YRD.•Formation mechanisms of secondary aerosol were studied by real-time measurement.•Secondary aerosol formation was enhanced by photochemical reactions.•New particle formation and growth was observed despite high aerosol loading.•Control measures for PM2.5 and O3 must be considered holistically in YRD.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>27418517</pmid><doi>10.1016/j.scitotenv.2016.06.212</doi><tpages>13</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0048-9697
ispartof The Science of the total environment, 2016-11, Vol.571, p.1454-1466
issn 0048-9697
1879-1026
language eng
recordid cdi_proquest_miscellaneous_1827908173
source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Aerosols - analysis
Air Pollutants - analysis
China
Environmental Monitoring
Gaseous Precursors
Ozone - analysis
Particle Size
Particulate Matter - analysis
Photochemical Oxidation
Photochemical Processes
PM2.5
Seasons
Secondary Aerosol Formation
Yangtze River Delta
title Intense secondary aerosol formation due to strong atmospheric photochemical reactions in summer: observations at a rural site in eastern Yangtze River Delta of China
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T23%3A02%3A03IST&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=Intense%20secondary%20aerosol%20formation%20due%20to%20strong%20atmospheric%20photochemical%20reactions%20in%20summer:%20observations%20at%20a%20rural%20site%20in%20eastern%20Yangtze%20River%20Delta%20of%20China&rft.jtitle=The%20Science%20of%20the%20total%20environment&rft.au=Wang,%20Dongfang&rft.date=2016-11-15&rft.volume=571&rft.spage=1454&rft.epage=1466&rft.pages=1454-1466&rft.issn=0048-9697&rft.eissn=1879-1026&rft_id=info:doi/10.1016/j.scitotenv.2016.06.212&rft_dat=%3Cproquest_cross%3E1827908173%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=1827908173&rft_id=info:pmid/27418517&rft_els_id=S0048969716314012&rfr_iscdi=true