Formation and growth rates of ultrafine atmospheric particles: a review of observations
Over the past decade, the formation and growth of nanometer-size atmospheric aerosol particles have been observed at a number of sites around the world. Measurements of particle formation have been performed on different platforms (ground, ships, aircraft) and over different time periods (campaign o...
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Veröffentlicht in: | Journal of aerosol science 2004-03, Vol.35 (2), p.143-176 |
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container_title | Journal of aerosol science |
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creator | Kulmala, M. Vehkamäki, H. Petäjä, T. Dal Maso, M. Lauri, A. Kerminen, V.-M. Birmili, W. McMurry, P.H. |
description | Over the past decade, the formation and growth of nanometer-size atmospheric aerosol particles have been observed at a number of sites around the world. Measurements of particle formation have been performed on different platforms (ground, ships, aircraft) and over different time periods (campaign or continuous-type measurements). The development during the 1990s of new instruments to measure nanoparticle size distributions and several gases that participate in nucleation have enabled these new discoveries. Measurements during nucleation episodes of evolving size distributions down to
3
nm
can be used to calculate the apparent source rate of 3-nm particles and the particle growth rate. We have collected existing data from the literature and data banks (campaigns and continuous measurements), representing more than 100 individual investigations. We conclude that the formation rate of 3-nm particles is often in the range 0.01–
10
cm
−3
s
−1
in the boundary layer. However, in urban areas formation rates are often higher than this (up to
100
cm
−3
s
−1
), and rates as high as 10
4–
10
5
cm
−3
s
−1
have been observed in coastal areas and industrial plumes. Typical particle growth rates are in the range 1–
20
nm
h
−1
in mid-latitudes depending on the temperature and the availability of condensable vapours. Over polar areas the growth rate can be as low as
0.1
nm
h
−1
. Because nucleation can lead to a significant increase in the number concentration of cloud condensation nuclei, global climate models will require reliable models for nucleation. |
doi_str_mv | 10.1016/j.jaerosci.2003.10.003 |
format | Article |
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3
nm
can be used to calculate the apparent source rate of 3-nm particles and the particle growth rate. We have collected existing data from the literature and data banks (campaigns and continuous measurements), representing more than 100 individual investigations. We conclude that the formation rate of 3-nm particles is often in the range 0.01–
10
cm
−3
s
−1
in the boundary layer. However, in urban areas formation rates are often higher than this (up to
100
cm
−3
s
−1
), and rates as high as 10
4–
10
5
cm
−3
s
−1
have been observed in coastal areas and industrial plumes. Typical particle growth rates are in the range 1–
20
nm
h
−1
in mid-latitudes depending on the temperature and the availability of condensable vapours. Over polar areas the growth rate can be as low as
0.1
nm
h
−1
. Because nucleation can lead to a significant increase in the number concentration of cloud condensation nuclei, global climate models will require reliable models for nucleation.</description><identifier>ISSN: 0021-8502</identifier><identifier>EISSN: 1879-1964</identifier><identifier>DOI: 10.1016/j.jaerosci.2003.10.003</identifier><identifier>CODEN: JALSB7</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Aerosols ; Atmospheric aerosols ; Chemistry ; Colloidal state and disperse state ; Condensation growth ; Exact sciences and technology ; General and physical chemistry ; Nucleation</subject><ispartof>Journal of aerosol science, 2004-03, Vol.35 (2), p.143-176</ispartof><rights>2003 Elsevier Science Ltd</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c437t-90a767ab31c04eb4ab26580a837d6cdd8a71071eb45970c5c42d0c7b58fb63e63</citedby><cites>FETCH-LOGICAL-c437t-90a767ab31c04eb4ab26580a837d6cdd8a71071eb45970c5c42d0c7b58fb63e63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0021850203004373$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15478561$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Kulmala, M.</creatorcontrib><creatorcontrib>Vehkamäki, H.</creatorcontrib><creatorcontrib>Petäjä, T.</creatorcontrib><creatorcontrib>Dal Maso, M.</creatorcontrib><creatorcontrib>Lauri, A.</creatorcontrib><creatorcontrib>Kerminen, V.-M.</creatorcontrib><creatorcontrib>Birmili, W.</creatorcontrib><creatorcontrib>McMurry, P.H.</creatorcontrib><title>Formation and growth rates of ultrafine atmospheric particles: a review of observations</title><title>Journal of aerosol science</title><description>Over the past decade, the formation and growth of nanometer-size atmospheric aerosol particles have been observed at a number of sites around the world. Measurements of particle formation have been performed on different platforms (ground, ships, aircraft) and over different time periods (campaign or continuous-type measurements). The development during the 1990s of new instruments to measure nanoparticle size distributions and several gases that participate in nucleation have enabled these new discoveries. Measurements during nucleation episodes of evolving size distributions down to
3
nm
can be used to calculate the apparent source rate of 3-nm particles and the particle growth rate. We have collected existing data from the literature and data banks (campaigns and continuous measurements), representing more than 100 individual investigations. We conclude that the formation rate of 3-nm particles is often in the range 0.01–
10
cm
−3
s
−1
in the boundary layer. However, in urban areas formation rates are often higher than this (up to
100
cm
−3
s
−1
), and rates as high as 10
4–
10
5
cm
−3
s
−1
have been observed in coastal areas and industrial plumes. Typical particle growth rates are in the range 1–
20
nm
h
−1
in mid-latitudes depending on the temperature and the availability of condensable vapours. Over polar areas the growth rate can be as low as
0.1
nm
h
−1
. Because nucleation can lead to a significant increase in the number concentration of cloud condensation nuclei, global climate models will require reliable models for nucleation.</description><subject>Aerosols</subject><subject>Atmospheric aerosols</subject><subject>Chemistry</subject><subject>Colloidal state and disperse state</subject><subject>Condensation growth</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Nucleation</subject><issn>0021-8502</issn><issn>1879-1964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqFkMFO4zAQhi0EEoXdV1j5AreUcRLbCScQgl0kJC6LOFoTZ7J1lcbFdot4e9wtiCOnXxp_84_8MfZLwFyAUBfL-RIp-GjdvASo8nCe44DNRKPbQrSqPmQzgFIUjYTymJ3EuAQA3Qo5Y893PqwwOT9xnHr-L_jXtOABE0XuB74ZU8DBTcQxrXxcLyg4y9cYkrMjxUuOPNDW0esO9l2ksP1fFn-wowHHSD8_8pQ93d3-vflTPDz-vr-5fihsXelUtIBaaewqYaGmrsauVLIBbCrdK9v3DWoBWuQX2Wqw0tZlD1Z3shk6VZGqTtn5vncd_MuGYjIrFy2NI07kN9EILSrdSJlBtQdtVhUDDWYd3ArDmxFgdh7N0nx6NDuPu3mOvHj2cQGjxXEIOFkXv7ZlnfuVyNzVnqP83awkmNxEk6XeBbLJ9N59d-od2jeNhA</recordid><startdate>200403</startdate><enddate>200403</enddate><creator>Kulmala, M.</creator><creator>Vehkamäki, H.</creator><creator>Petäjä, T.</creator><creator>Dal Maso, M.</creator><creator>Lauri, A.</creator><creator>Kerminen, V.-M.</creator><creator>Birmili, W.</creator><creator>McMurry, P.H.</creator><general>Elsevier Ltd</general><general>Elsevier Science</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TG</scope><scope>KL.</scope></search><sort><creationdate>200403</creationdate><title>Formation and growth rates of ultrafine atmospheric particles: a review of observations</title><author>Kulmala, M. ; Vehkamäki, H. ; Petäjä, T. ; Dal Maso, M. ; Lauri, A. ; Kerminen, V.-M. ; Birmili, W. ; McMurry, P.H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c437t-90a767ab31c04eb4ab26580a837d6cdd8a71071eb45970c5c42d0c7b58fb63e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Aerosols</topic><topic>Atmospheric aerosols</topic><topic>Chemistry</topic><topic>Colloidal state and disperse state</topic><topic>Condensation growth</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Nucleation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kulmala, M.</creatorcontrib><creatorcontrib>Vehkamäki, H.</creatorcontrib><creatorcontrib>Petäjä, T.</creatorcontrib><creatorcontrib>Dal Maso, M.</creatorcontrib><creatorcontrib>Lauri, A.</creatorcontrib><creatorcontrib>Kerminen, V.-M.</creatorcontrib><creatorcontrib>Birmili, W.</creatorcontrib><creatorcontrib>McMurry, P.H.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><jtitle>Journal of aerosol science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kulmala, M.</au><au>Vehkamäki, H.</au><au>Petäjä, T.</au><au>Dal Maso, M.</au><au>Lauri, A.</au><au>Kerminen, V.-M.</au><au>Birmili, W.</au><au>McMurry, P.H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Formation and growth rates of ultrafine atmospheric particles: a review of observations</atitle><jtitle>Journal of aerosol science</jtitle><date>2004-03</date><risdate>2004</risdate><volume>35</volume><issue>2</issue><spage>143</spage><epage>176</epage><pages>143-176</pages><issn>0021-8502</issn><eissn>1879-1964</eissn><coden>JALSB7</coden><abstract>Over the past decade, the formation and growth of nanometer-size atmospheric aerosol particles have been observed at a number of sites around the world. Measurements of particle formation have been performed on different platforms (ground, ships, aircraft) and over different time periods (campaign or continuous-type measurements). The development during the 1990s of new instruments to measure nanoparticle size distributions and several gases that participate in nucleation have enabled these new discoveries. Measurements during nucleation episodes of evolving size distributions down to
3
nm
can be used to calculate the apparent source rate of 3-nm particles and the particle growth rate. We have collected existing data from the literature and data banks (campaigns and continuous measurements), representing more than 100 individual investigations. We conclude that the formation rate of 3-nm particles is often in the range 0.01–
10
cm
−3
s
−1
in the boundary layer. However, in urban areas formation rates are often higher than this (up to
100
cm
−3
s
−1
), and rates as high as 10
4–
10
5
cm
−3
s
−1
have been observed in coastal areas and industrial plumes. Typical particle growth rates are in the range 1–
20
nm
h
−1
in mid-latitudes depending on the temperature and the availability of condensable vapours. Over polar areas the growth rate can be as low as
0.1
nm
h
−1
. Because nucleation can lead to a significant increase in the number concentration of cloud condensation nuclei, global climate models will require reliable models for nucleation.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.jaerosci.2003.10.003</doi><tpages>34</tpages></addata></record> |
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subjects | Aerosols Atmospheric aerosols Chemistry Colloidal state and disperse state Condensation growth Exact sciences and technology General and physical chemistry Nucleation |
title | Formation and growth rates of ultrafine atmospheric particles: a review of observations |
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