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Measurement report: Online measurement of gas-phase nitrated phenols utilizing a CI-LToF-MS: primary sources and secondary formation
To investigate the composition, variation, and sources of nitrated phenols (NPs) in the winter of Beijing, gas-phase NPs were measured by a chemical ionization long time-of-flight mass spectrometer (CI-LToF-MS). A box model was applied to simulate the secondary formation process of NPs. In addition,...
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Published in: | Atmospheric chemistry and physics 2021-05, Vol.21 (10), p.7917-7932 |
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creator | Song, Kai Guo, Song Wang, Haichao Yu, Ying Wang, Hui Tang, Rongzhi Xia, Shiyong Gong, Yuanzheng Wan, Zichao Lv, Daqi Tan, Rui Zhu, Wenfei Shen, Ruizhe Li, Xin Yu, Xuena Chen, Shiyi Zeng, Liming Huang, Xiaofeng |
description | To investigate the composition, variation, and sources of
nitrated phenols (NPs) in the winter of Beijing, gas-phase NPs were measured
by a chemical ionization long time-of-flight mass spectrometer (CI-LToF-MS). A
box model was applied to simulate the secondary formation process of NPs. In
addition, the primary sources of NPs were resolved by a non-negative matrix
factorization (NMF) model. Our results showed that secondary formation
contributed 38 %, 9 %, 5 %, 17 %,
and almost 100 % of the nitrophenol (NP), methyl-nitrophenol (MNP),
dinitrophenol (DNP), methyl-dinitrophenol (MDNP or DNOC), and
dimethyl-nitrophenol (DMNP) concentrations. The phenol–OH reaction was the
predominant loss pathway (46.7 %) during the heavy pollution
episode, which produced the phenoxy radical (C6H5O). The phenoxy
radical consequently reacted with NO2 and produced nitrophenol. By
estimating the primarily emitted phenol from the ratio of phenol/CO from
freshly emitted vehicle exhaust, this study proposed that oxidation of primary
phenol contributes much more nitrophenol (37 %) than that from
benzene oxidation (50 %) to the gas-phase NPs. The industry source
contributed 30 % and 9 % to DNP and MDNP, respectively,
which was non-negligible. The concentration weighted trajectory (CWT) analysis
demonstrated that regional transport from provinces that surround the Yellow
and Bohai seas contributed more primary NPs to Beijing. Both primary sources
and secondary formation at either local or regional scale should be considered
when making control policies of NPs. |
doi_str_mv | 10.5194/acp-21-7917-2021 |
format | article |
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nitrated phenols (NPs) in the winter of Beijing, gas-phase NPs were measured
by a chemical ionization long time-of-flight mass spectrometer (CI-LToF-MS). A
box model was applied to simulate the secondary formation process of NPs. In
addition, the primary sources of NPs were resolved by a non-negative matrix
factorization (NMF) model. Our results showed that secondary formation
contributed 38 %, 9 %, 5 %, 17 %,
and almost 100 % of the nitrophenol (NP), methyl-nitrophenol (MNP),
dinitrophenol (DNP), methyl-dinitrophenol (MDNP or DNOC), and
dimethyl-nitrophenol (DMNP) concentrations. The phenol–OH reaction was the
predominant loss pathway (46.7 %) during the heavy pollution
episode, which produced the phenoxy radical (C6H5O). The phenoxy
radical consequently reacted with NO2 and produced nitrophenol. By
estimating the primarily emitted phenol from the ratio of phenol/CO from
freshly emitted vehicle exhaust, this study proposed that oxidation of primary
phenol contributes much more nitrophenol (37 %) than that from
benzene oxidation (<1 %) in the winter of Beijing. The latter
pathway was widely used in models and might lead to great uncertainties. The
source apportionment results by NMF indicated the importance of combustion
sources (>50 %) to the gas-phase NPs. The industry source
contributed 30 % and 9 % to DNP and MDNP, respectively,
which was non-negligible. The concentration weighted trajectory (CWT) analysis
demonstrated that regional transport from provinces that surround the Yellow
and Bohai seas contributed more primary NPs to Beijing. Both primary sources
and secondary formation at either local or regional scale should be considered
when making control policies of NPs.</description><identifier>ISSN: 1680-7324</identifier><identifier>ISSN: 1680-7316</identifier><identifier>EISSN: 1680-7324</identifier><identifier>DOI: 10.5194/acp-21-7917-2021</identifier><language>eng</language><publisher>Katlenburg-Lindau: Copernicus GmbH</publisher><subject>Analysis ; Benzene ; Calibration ; Chromatography ; Hydrocarbons ; Ionization ; Mass spectrometry ; Measurement ; Nitrates ; Nitrogen dioxide ; Nitrophenol ; Oxidation ; Phenols ; Pollutants ; Pollution ; Trajectory analysis ; Vehicle emissions ; VOCs ; Volatile organic compounds ; Winter</subject><ispartof>Atmospheric chemistry and physics, 2021-05, Vol.21 (10), p.7917-7932</ispartof><rights>COPYRIGHT 2021 Copernicus GmbH</rights><rights>2021. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c480t-7a570ad812ac9fa3ef150acea66ad27c27ca375551e2c60738f0bbc217f8a12c3</citedby><cites>FETCH-LOGICAL-c480t-7a570ad812ac9fa3ef150acea66ad27c27ca375551e2c60738f0bbc217f8a12c3</cites><orcidid>0000-0002-9661-2313 ; 0000-0001-6161-1874 ; 0000-0003-2322-4069</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2531519254/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2531519254?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,864,2102,25753,27924,27925,37012,44590,75126</link.rule.ids></links><search><creatorcontrib>Song, Kai</creatorcontrib><creatorcontrib>Guo, Song</creatorcontrib><creatorcontrib>Wang, Haichao</creatorcontrib><creatorcontrib>Yu, Ying</creatorcontrib><creatorcontrib>Wang, Hui</creatorcontrib><creatorcontrib>Tang, Rongzhi</creatorcontrib><creatorcontrib>Xia, Shiyong</creatorcontrib><creatorcontrib>Gong, Yuanzheng</creatorcontrib><creatorcontrib>Wan, Zichao</creatorcontrib><creatorcontrib>Lv, Daqi</creatorcontrib><creatorcontrib>Tan, Rui</creatorcontrib><creatorcontrib>Zhu, Wenfei</creatorcontrib><creatorcontrib>Shen, Ruizhe</creatorcontrib><creatorcontrib>Li, Xin</creatorcontrib><creatorcontrib>Yu, Xuena</creatorcontrib><creatorcontrib>Chen, Shiyi</creatorcontrib><creatorcontrib>Zeng, Liming</creatorcontrib><creatorcontrib>Huang, Xiaofeng</creatorcontrib><title>Measurement report: Online measurement of gas-phase nitrated phenols utilizing a CI-LToF-MS: primary sources and secondary formation</title><title>Atmospheric chemistry and physics</title><description>To investigate the composition, variation, and sources of
nitrated phenols (NPs) in the winter of Beijing, gas-phase NPs were measured
by a chemical ionization long time-of-flight mass spectrometer (CI-LToF-MS). A
box model was applied to simulate the secondary formation process of NPs. In
addition, the primary sources of NPs were resolved by a non-negative matrix
factorization (NMF) model. Our results showed that secondary formation
contributed 38 %, 9 %, 5 %, 17 %,
and almost 100 % of the nitrophenol (NP), methyl-nitrophenol (MNP),
dinitrophenol (DNP), methyl-dinitrophenol (MDNP or DNOC), and
dimethyl-nitrophenol (DMNP) concentrations. The phenol–OH reaction was the
predominant loss pathway (46.7 %) during the heavy pollution
episode, which produced the phenoxy radical (C6H5O). The phenoxy
radical consequently reacted with NO2 and produced nitrophenol. By
estimating the primarily emitted phenol from the ratio of phenol/CO from
freshly emitted vehicle exhaust, this study proposed that oxidation of primary
phenol contributes much more nitrophenol (37 %) than that from
benzene oxidation (<1 %) in the winter of Beijing. The latter
pathway was widely used in models and might lead to great uncertainties. The
source apportionment results by NMF indicated the importance of combustion
sources (>50 %) to the gas-phase NPs. The industry source
contributed 30 % and 9 % to DNP and MDNP, respectively,
which was non-negligible. The concentration weighted trajectory (CWT) analysis
demonstrated that regional transport from provinces that surround the Yellow
and Bohai seas contributed more primary NPs to Beijing. Both primary sources
and secondary formation at either local or regional scale should be considered
when making control policies of NPs.</description><subject>Analysis</subject><subject>Benzene</subject><subject>Calibration</subject><subject>Chromatography</subject><subject>Hydrocarbons</subject><subject>Ionization</subject><subject>Mass spectrometry</subject><subject>Measurement</subject><subject>Nitrates</subject><subject>Nitrogen dioxide</subject><subject>Nitrophenol</subject><subject>Oxidation</subject><subject>Phenols</subject><subject>Pollutants</subject><subject>Pollution</subject><subject>Trajectory analysis</subject><subject>Vehicle emissions</subject><subject>VOCs</subject><subject>Volatile organic compounds</subject><subject>Winter</subject><issn>1680-7324</issn><issn>1680-7316</issn><issn>1680-7324</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUkFrFDEUHkTBWr17DHjykJpkJpOZ3spidWFLwdZzeJt5mWaZScYkC-rZH27WLdoFSSCPL9_78t7LV1VvObuQvG8-gFmo4FT1XFHBBH9WnfG2Y1TVonn-JH5ZvUppx5iQjDdn1a8bhLSPOKPPJOISYr4kt35yHsn85CpYMkKiywMkJN7lCBkHsjygD1Mi--wm99P5kQBZrenmPlzTm7tLskQ3Q_xBUthHg4mAH0hCE_xwQG2IM2QX_OvqhYUp4ZvH87z6ev3xfvWZbm4_rVdXG2qajmWqQCoGQ8cFmN5CjZZLBgahbWEQypQNtZJSchSmZaruLNtujeDKdsCFqc-r9VF3CLDTj8XpAE7_AUIcNcTszIQaRNdzJrt2aLDhfQ-N7WV5vkPcDpINRevdUWuJ4dseU9a70qQv5Wsha17-RMjmH2uEIuq8DWVyZnbJ6Ku2FX1b90oV1sV_WGUNOLsyLbSu4CcJ708SCifj9zzCPiW9vvtyymVHrokhpYj2b-Oc6YN1dLGOFlwfrKMP1ql_A2iRtkI</recordid><startdate>20210525</startdate><enddate>20210525</enddate><creator>Song, Kai</creator><creator>Guo, Song</creator><creator>Wang, Haichao</creator><creator>Yu, 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report: Online measurement of gas-phase nitrated phenols utilizing a CI-LToF-MS: primary sources and secondary formation</title><author>Song, Kai ; Guo, Song ; Wang, Haichao ; Yu, Ying ; Wang, Hui ; Tang, Rongzhi ; Xia, Shiyong ; Gong, Yuanzheng ; Wan, Zichao ; Lv, Daqi ; Tan, Rui ; Zhu, Wenfei ; Shen, Ruizhe ; Li, Xin ; Yu, Xuena ; Chen, Shiyi ; Zeng, Liming ; Huang, Xiaofeng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c480t-7a570ad812ac9fa3ef150acea66ad27c27ca375551e2c60738f0bbc217f8a12c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Analysis</topic><topic>Benzene</topic><topic>Calibration</topic><topic>Chromatography</topic><topic>Hydrocarbons</topic><topic>Ionization</topic><topic>Mass spectrometry</topic><topic>Measurement</topic><topic>Nitrates</topic><topic>Nitrogen dioxide</topic><topic>Nitrophenol</topic><topic>Oxidation</topic><topic>Phenols</topic><topic>Pollutants</topic><topic>Pollution</topic><topic>Trajectory analysis</topic><topic>Vehicle emissions</topic><topic>VOCs</topic><topic>Volatile organic compounds</topic><topic>Winter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Song, Kai</creatorcontrib><creatorcontrib>Guo, Song</creatorcontrib><creatorcontrib>Wang, Haichao</creatorcontrib><creatorcontrib>Yu, Ying</creatorcontrib><creatorcontrib>Wang, Hui</creatorcontrib><creatorcontrib>Tang, Rongzhi</creatorcontrib><creatorcontrib>Xia, Shiyong</creatorcontrib><creatorcontrib>Gong, Yuanzheng</creatorcontrib><creatorcontrib>Wan, Zichao</creatorcontrib><creatorcontrib>Lv, Daqi</creatorcontrib><creatorcontrib>Tan, Rui</creatorcontrib><creatorcontrib>Zhu, Wenfei</creatorcontrib><creatorcontrib>Shen, Ruizhe</creatorcontrib><creatorcontrib>Li, Xin</creatorcontrib><creatorcontrib>Yu, 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Wenfei</au><au>Shen, Ruizhe</au><au>Li, Xin</au><au>Yu, Xuena</au><au>Chen, Shiyi</au><au>Zeng, Liming</au><au>Huang, Xiaofeng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Measurement report: Online measurement of gas-phase nitrated phenols utilizing a CI-LToF-MS: primary sources and secondary formation</atitle><jtitle>Atmospheric chemistry and physics</jtitle><date>2021-05-25</date><risdate>2021</risdate><volume>21</volume><issue>10</issue><spage>7917</spage><epage>7932</epage><pages>7917-7932</pages><issn>1680-7324</issn><issn>1680-7316</issn><eissn>1680-7324</eissn><abstract>To investigate the composition, variation, and sources of
nitrated phenols (NPs) in the winter of Beijing, gas-phase NPs were measured
by a chemical ionization long time-of-flight mass spectrometer (CI-LToF-MS). A
box model was applied to simulate the secondary formation process of NPs. In
addition, the primary sources of NPs were resolved by a non-negative matrix
factorization (NMF) model. Our results showed that secondary formation
contributed 38 %, 9 %, 5 %, 17 %,
and almost 100 % of the nitrophenol (NP), methyl-nitrophenol (MNP),
dinitrophenol (DNP), methyl-dinitrophenol (MDNP or DNOC), and
dimethyl-nitrophenol (DMNP) concentrations. The phenol–OH reaction was the
predominant loss pathway (46.7 %) during the heavy pollution
episode, which produced the phenoxy radical (C6H5O). The phenoxy
radical consequently reacted with NO2 and produced nitrophenol. By
estimating the primarily emitted phenol from the ratio of phenol/CO from
freshly emitted vehicle exhaust, this study proposed that oxidation of primary
phenol contributes much more nitrophenol (37 %) than that from
benzene oxidation (<1 %) in the winter of Beijing. The latter
pathway was widely used in models and might lead to great uncertainties. The
source apportionment results by NMF indicated the importance of combustion
sources (>50 %) to the gas-phase NPs. The industry source
contributed 30 % and 9 % to DNP and MDNP, respectively,
which was non-negligible. The concentration weighted trajectory (CWT) analysis
demonstrated that regional transport from provinces that surround the Yellow
and Bohai seas contributed more primary NPs to Beijing. Both primary sources
and secondary formation at either local or regional scale should be considered
when making control policies of NPs.</abstract><cop>Katlenburg-Lindau</cop><pub>Copernicus GmbH</pub><doi>10.5194/acp-21-7917-2021</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0002-9661-2313</orcidid><orcidid>https://orcid.org/0000-0001-6161-1874</orcidid><orcidid>https://orcid.org/0000-0003-2322-4069</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Benzene Calibration Chromatography Hydrocarbons Ionization Mass spectrometry Measurement Nitrates Nitrogen dioxide Nitrophenol Oxidation Phenols Pollutants Pollution Trajectory analysis Vehicle emissions VOCs Volatile organic compounds Winter |
title | Measurement report: Online measurement of gas-phase nitrated phenols utilizing a CI-LToF-MS: primary sources and secondary formation |
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