Size and Composition Biases on the Detection of Individual Ultrafine Particles by Aerosol Mass Spectrometry
Aerosol mass spectrometers allow particles to be counted on the basis of size and chemical composition. In most instruments, individual particles are ablated with a pulsed laser to obtain a mass spectrum. Using this method to characterize ambient aerosols requires an understanding of biases induced...
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Veröffentlicht in: | Environmental science & technology 2000-12, Vol.34 (23), p.4887-4893 |
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description | Aerosol mass spectrometers allow particles to be counted on the basis of size and chemical composition. In most instruments, individual particles are ablated with a pulsed laser to obtain a mass spectrum. Using this method to characterize ambient aerosols requires an understanding of biases induced by the measurement process. For particles less than 200 nm diameter, the efficiency of detection is shown to be dependent on both size and composition. These dependencies arise from the transmission characteristics of the particle inlet and the intrinsic ability of a particle to be vaporized and ionized. The relative contributions of each are determined for a series of atmospherically relevant test aerosols. Small particles are generally more difficult to detect and analyze than large particles because they are more difficult to focus through the inlet into a tight beam and because they are more difficult to ablate. Particles composed of polycyclic aromatic hydrocarbons, ammonium nitrate, and alkali metal ions are efficiently ablated by laser ablation. Aliphatic organics are less efficiently ablated, and ammonium sulfate is very difficult to detect in a positive ion spectrum. The mass spectra of ultrafine particles show extensive fragmentation, making it difficult to distinguish aliphatic and aromatic components. However, organic particles may be classified on the basis of inorganic impurities. Initial field measurements of ambient ultrafine particles are consistent with these conclusions. |
doi_str_mv | 10.1021/es001323y |
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In most instruments, individual particles are ablated with a pulsed laser to obtain a mass spectrum. Using this method to characterize ambient aerosols requires an understanding of biases induced by the measurement process. For particles less than 200 nm diameter, the efficiency of detection is shown to be dependent on both size and composition. These dependencies arise from the transmission characteristics of the particle inlet and the intrinsic ability of a particle to be vaporized and ionized. The relative contributions of each are determined for a series of atmospherically relevant test aerosols. Small particles are generally more difficult to detect and analyze than large particles because they are more difficult to focus through the inlet into a tight beam and because they are more difficult to ablate. Particles composed of polycyclic aromatic hydrocarbons, ammonium nitrate, and alkali metal ions are efficiently ablated by laser ablation. Aliphatic organics are less efficiently ablated, and ammonium sulfate is very difficult to detect in a positive ion spectrum. The mass spectra of ultrafine particles show extensive fragmentation, making it difficult to distinguish aliphatic and aromatic components. However, organic particles may be classified on the basis of inorganic impurities. 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Sci. Technol</addtitle><description>Aerosol mass spectrometers allow particles to be counted on the basis of size and chemical composition. In most instruments, individual particles are ablated with a pulsed laser to obtain a mass spectrum. Using this method to characterize ambient aerosols requires an understanding of biases induced by the measurement process. For particles less than 200 nm diameter, the efficiency of detection is shown to be dependent on both size and composition. These dependencies arise from the transmission characteristics of the particle inlet and the intrinsic ability of a particle to be vaporized and ionized. The relative contributions of each are determined for a series of atmospherically relevant test aerosols. Small particles are generally more difficult to detect and analyze than large particles because they are more difficult to focus through the inlet into a tight beam and because they are more difficult to ablate. Particles composed of polycyclic aromatic hydrocarbons, ammonium nitrate, and alkali metal ions are efficiently ablated by laser ablation. Aliphatic organics are less efficiently ablated, and ammonium sulfate is very difficult to detect in a positive ion spectrum. The mass spectra of ultrafine particles show extensive fragmentation, making it difficult to distinguish aliphatic and aromatic components. However, organic particles may be classified on the basis of inorganic impurities. Initial field measurements of ambient ultrafine particles are consistent with these conclusions.</description><subject>Aerosols</subject><subject>Aerosols and foams</subject><subject>Analysis methods</subject><subject>Analytical chemistry</subject><subject>Applied sciences</subject><subject>Atmospheric pollution</subject><subject>Chemicals</subject><subject>Chemistry</subject><subject>Colloidal state and disperse state</subject><subject>Environmental monitoring</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Instruments, apparatus, components and techniques common to several branches of physics and astronomy</subject><subject>Mass spectrometers and related techniques</subject><subject>Physics</subject><subject>Pollution</subject><subject>Scientific imaging</subject><subject>Spectrometric and optical methods</subject><issn>0013-936X</issn><issn>1520-5851</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNplkE1vEzEQhi0EEqFw4B9YIA4cFsZ21vYeS6BQqYWitCo3a-qdFW4362A7iPDrcUgVDpxmNPO873ww9lzAGwFSvKUMIJRU2wdsJloJTWtb8ZDNdtWmU_rbY_Yk51sAkArsjN0tw2_iOPV8EVfrmEMJceLvAmbKvGblO_H3VMj_rceBn059-Bn6DY78aiwJhzARv8BUgh-r5GbLjynFHEd-jjnz5bpKU1xRSdun7NGAY6Zn9_GIXZ18uFx8as6-fDxdHJ81qFoojTGSDAhrhuGGrJx77LXuNIFHY3vClrQFLdH2nUbQvp0bpXynrMA5QofqiL3Y-65T_LGhXNxt3KSpjnT1aCGtnusKvd5Dvm6bEw1uncIK09YJcLtXusMrK_vy3hCzx3FIOPmQDwLbSg07x2ZPhVzo16GL6c5po0zrLi-W7vzryWdz3V27ReVf7Xn0-d-G_0__A-82jpU</recordid><startdate>20001201</startdate><enddate>20001201</enddate><creator>Kane, David B</creator><creator>Johnston, Murray V</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</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></search><sort><creationdate>20001201</creationdate><title>Size and Composition Biases on the Detection of Individual Ultrafine Particles by Aerosol Mass Spectrometry</title><author>Kane, David B ; Johnston, Murray V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a350t-772e70187ffbe824cad6696e0ca78dea5e68062a8d96a06c54733c9381a4a09a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Aerosols</topic><topic>Aerosols and foams</topic><topic>Analysis methods</topic><topic>Analytical chemistry</topic><topic>Applied sciences</topic><topic>Atmospheric pollution</topic><topic>Chemicals</topic><topic>Chemistry</topic><topic>Colloidal state and disperse state</topic><topic>Environmental monitoring</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Instruments, apparatus, components and techniques common to several branches of physics and astronomy</topic><topic>Mass spectrometers and related techniques</topic><topic>Physics</topic><topic>Pollution</topic><topic>Scientific imaging</topic><topic>Spectrometric and optical methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kane, David B</creatorcontrib><creatorcontrib>Johnston, Murray V</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</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><jtitle>Environmental science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kane, David B</au><au>Johnston, Murray V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Size and Composition Biases on the Detection of Individual Ultrafine Particles by Aerosol Mass Spectrometry</atitle><jtitle>Environmental science & technology</jtitle><addtitle>Environ. 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subjects | Aerosols Aerosols and foams Analysis methods Analytical chemistry Applied sciences Atmospheric pollution Chemicals Chemistry Colloidal state and disperse state Environmental monitoring Exact sciences and technology General and physical chemistry Instruments, apparatus, components and techniques common to several branches of physics and astronomy Mass spectrometers and related techniques Physics Pollution Scientific imaging Spectrometric and optical methods |
title | Size and Composition Biases on the Detection of Individual Ultrafine Particles by Aerosol Mass Spectrometry |
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