Real-time separation of aerosolized Staphylococcus epidermidis and polystyrene latex particles with similar size distributions
For rapid and effective detection of airborne microorganisms, it is preferable to remove dust particles during the air sampling process because they can reduce the detection accuracy of measurements. In this study, a methodology of real-time separation ofaerosolized Staphylococcus epidermidis (S. ep...
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Veröffentlicht in: | Aerosol science and technology 2017-12, Vol.51 (12), p.1389-1397 |
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creator | Mohamadi Nasrabadi, Ali Han, Jang Seop Massoudi Farid, Milad Lee, Sang-Gu Hwang, Jungho |
description | For rapid and effective detection of airborne microorganisms, it is preferable to remove dust particles during the air sampling process because they can reduce the detection accuracy of measurements. In this study, a methodology of real-time separation ofaerosolized Staphylococcus epidermidis (S. epidermidis) andpolystyrene latex (PSL) particles of similar size was investigated. These two species represent biological and non-biological particles, respectively. Due to their different relative permittivities, they grasp different numbers of air ions under corona discharge. After these charged particles enter a mobility analyzer with airflow, in which an electric field is applied perpendicular to the airflow, the S. epidermidis and PSL particles separate, due to the difference in their electric mobilities, and exit through two different outlets. Purities and recoveries for S. epidermidis and PSLat their respective outlets were determined with measurements of aerosol number concentrations and ATP bioluminescence intensities at the inlet and two outlets. The results were that purities for PSL and S. epidermidis were 70% and 80%, respectively. This methodology provides a rapid and simple way to increase the detection accuracy of bacterial agents in air.
Copyright © 2017 American Association for Aerosol Research |
doi_str_mv | 10.1080/02786826.2017.1350257 |
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Copyright © 2017 American Association for Aerosol Research</description><identifier>ISSN: 0278-6826</identifier><identifier>EISSN: 1521-7388</identifier><identifier>DOI: 10.1080/02786826.2017.1350257</identifier><language>eng</language><publisher>New York: Taylor & Francis</publisher><subject>Aerosol research ; Aerosols ; Air flow ; Air sampling ; Airborne microorganisms ; Bacteria ; Bioluminescence ; Charged particles ; Charging ; Corona ; Disinfection & disinfectants ; Dust particles ; Electric fields ; Latex ; Microorganisms ; Outlets ; Particle size ; Polystyrene resins ; Real time ; Separation ; Tiina Reponen</subject><ispartof>Aerosol science and technology, 2017-12, Vol.51 (12), p.1389-1397</ispartof><rights>2017 American Association for Aerosol Research 2017</rights><rights>2017 American Association for Aerosol Research</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c385t-14cdb4f8c8990e3cf6621ad5f9351fd9c05de35f1921cbd8b5fe960da2ebadc43</citedby><cites>FETCH-LOGICAL-c385t-14cdb4f8c8990e3cf6621ad5f9351fd9c05de35f1921cbd8b5fe960da2ebadc43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Mohamadi Nasrabadi, Ali</creatorcontrib><creatorcontrib>Han, Jang Seop</creatorcontrib><creatorcontrib>Massoudi Farid, Milad</creatorcontrib><creatorcontrib>Lee, Sang-Gu</creatorcontrib><creatorcontrib>Hwang, Jungho</creatorcontrib><title>Real-time separation of aerosolized Staphylococcus epidermidis and polystyrene latex particles with similar size distributions</title><title>Aerosol science and technology</title><description>For rapid and effective detection of airborne microorganisms, it is preferable to remove dust particles during the air sampling process because they can reduce the detection accuracy of measurements. In this study, a methodology of real-time separation ofaerosolized Staphylococcus epidermidis (S. epidermidis) andpolystyrene latex (PSL) particles of similar size was investigated. These two species represent biological and non-biological particles, respectively. Due to their different relative permittivities, they grasp different numbers of air ions under corona discharge. After these charged particles enter a mobility analyzer with airflow, in which an electric field is applied perpendicular to the airflow, the S. epidermidis and PSL particles separate, due to the difference in their electric mobilities, and exit through two different outlets. Purities and recoveries for S. epidermidis and PSLat their respective outlets were determined with measurements of aerosol number concentrations and ATP bioluminescence intensities at the inlet and two outlets. The results were that purities for PSL and S. epidermidis were 70% and 80%, respectively. This methodology provides a rapid and simple way to increase the detection accuracy of bacterial agents in air.
Copyright © 2017 American Association for Aerosol Research</description><subject>Aerosol research</subject><subject>Aerosols</subject><subject>Air flow</subject><subject>Air sampling</subject><subject>Airborne microorganisms</subject><subject>Bacteria</subject><subject>Bioluminescence</subject><subject>Charged particles</subject><subject>Charging</subject><subject>Corona</subject><subject>Disinfection & disinfectants</subject><subject>Dust particles</subject><subject>Electric fields</subject><subject>Latex</subject><subject>Microorganisms</subject><subject>Outlets</subject><subject>Particle size</subject><subject>Polystyrene resins</subject><subject>Real time</subject><subject>Separation</subject><subject>Tiina Reponen</subject><issn>0278-6826</issn><issn>1521-7388</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kEtrGzEUhUVJoU7Sn1AQdD2OHtaMZtcS8oJAoU3XQiNdYQXNaCrJOPaiv70a7G6zupvvnMP9EPpCyZoSSW4I62QrWbtmhHZrygVhovuAVlQw2nRcygu0WphmgT6hy5xfCakooyv09yfo0BQ_As4w66SLjxOODmtIMcfgj2Dxr6Ln7SFEE43ZZQyzt5BGb33GerJ4juGQyyHBBDjoAm-4FhVvAmS892WLsx990KneI-CaKskPu2UoX6OPTocMn8_3Cv2-v3u5fWyefzw83X5_bgyXojR0Y-ywcdLIvifAjWtbRrUVrueCOtsbIixw4WjPqBmsHISDviVWMxi0NRt-hb6eeucU_-wgF_Uad2mqk4r2HRN8QzmplDhRpv6eEzg1Jz_qdFCUqEW1-q9aLarVWXXNfTvl_ORiGvU-pmBV0VVZcklPxmfF36_4B0VtihY</recordid><startdate>20171202</startdate><enddate>20171202</enddate><creator>Mohamadi Nasrabadi, Ali</creator><creator>Han, Jang Seop</creator><creator>Massoudi Farid, Milad</creator><creator>Lee, Sang-Gu</creator><creator>Hwang, Jungho</creator><general>Taylor & Francis</general><general>Taylor & Francis Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7TB</scope><scope>7TG</scope><scope>8FD</scope><scope>FR3</scope><scope>KL.</scope></search><sort><creationdate>20171202</creationdate><title>Real-time separation of aerosolized Staphylococcus epidermidis and polystyrene latex particles with similar size distributions</title><author>Mohamadi Nasrabadi, Ali ; Han, Jang Seop ; Massoudi Farid, Milad ; Lee, Sang-Gu ; Hwang, Jungho</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c385t-14cdb4f8c8990e3cf6621ad5f9351fd9c05de35f1921cbd8b5fe960da2ebadc43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Aerosol research</topic><topic>Aerosols</topic><topic>Air flow</topic><topic>Air sampling</topic><topic>Airborne microorganisms</topic><topic>Bacteria</topic><topic>Bioluminescence</topic><topic>Charged particles</topic><topic>Charging</topic><topic>Corona</topic><topic>Disinfection & disinfectants</topic><topic>Dust particles</topic><topic>Electric fields</topic><topic>Latex</topic><topic>Microorganisms</topic><topic>Outlets</topic><topic>Particle size</topic><topic>Polystyrene resins</topic><topic>Real time</topic><topic>Separation</topic><topic>Tiina Reponen</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mohamadi Nasrabadi, Ali</creatorcontrib><creatorcontrib>Han, Jang Seop</creatorcontrib><creatorcontrib>Massoudi Farid, Milad</creatorcontrib><creatorcontrib>Lee, Sang-Gu</creatorcontrib><creatorcontrib>Hwang, Jungho</creatorcontrib><collection>CrossRef</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><jtitle>Aerosol science and technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mohamadi Nasrabadi, Ali</au><au>Han, Jang Seop</au><au>Massoudi Farid, Milad</au><au>Lee, Sang-Gu</au><au>Hwang, Jungho</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Real-time separation of aerosolized Staphylococcus epidermidis and polystyrene latex particles with similar size distributions</atitle><jtitle>Aerosol science and technology</jtitle><date>2017-12-02</date><risdate>2017</risdate><volume>51</volume><issue>12</issue><spage>1389</spage><epage>1397</epage><pages>1389-1397</pages><issn>0278-6826</issn><eissn>1521-7388</eissn><abstract>For rapid and effective detection of airborne microorganisms, it is preferable to remove dust particles during the air sampling process because they can reduce the detection accuracy of measurements. In this study, a methodology of real-time separation ofaerosolized Staphylococcus epidermidis (S. epidermidis) andpolystyrene latex (PSL) particles of similar size was investigated. These two species represent biological and non-biological particles, respectively. Due to their different relative permittivities, they grasp different numbers of air ions under corona discharge. After these charged particles enter a mobility analyzer with airflow, in which an electric field is applied perpendicular to the airflow, the S. epidermidis and PSL particles separate, due to the difference in their electric mobilities, and exit through two different outlets. Purities and recoveries for S. epidermidis and PSLat their respective outlets were determined with measurements of aerosol number concentrations and ATP bioluminescence intensities at the inlet and two outlets. The results were that purities for PSL and S. epidermidis were 70% and 80%, respectively. This methodology provides a rapid and simple way to increase the detection accuracy of bacterial agents in air.
Copyright © 2017 American Association for Aerosol Research</abstract><cop>New York</cop><pub>Taylor & Francis</pub><doi>10.1080/02786826.2017.1350257</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aerosol research Aerosols Air flow Air sampling Airborne microorganisms Bacteria Bioluminescence Charged particles Charging Corona Disinfection & disinfectants Dust particles Electric fields Latex Microorganisms Outlets Particle size Polystyrene resins Real time Separation Tiina Reponen |
title | Real-time separation of aerosolized Staphylococcus epidermidis and polystyrene latex particles with similar size distributions |
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