Please use this identifier to cite or link to this item:
https://doi.org/10.5194/amt-6-3211-2013
DC Field | Value | |
---|---|---|
dc.title | High-resolution chemical ionization mass spectrometry (ToF-CIMS): Application to study SOA composition and processing | |
dc.contributor.author | Aljawhary, D | |
dc.contributor.author | Lee, A.K.Y | |
dc.contributor.author | Abbatt, J.P.D | |
dc.date.accessioned | 2020-11-10T00:29:07Z | |
dc.date.available | 2020-11-10T00:29:07Z | |
dc.date.issued | 2013 | |
dc.identifier.citation | Aljawhary, D, Lee, A.K.Y, Abbatt, J.P.D (2013). High-resolution chemical ionization mass spectrometry (ToF-CIMS): Application to study SOA composition and processing. Atmospheric Measurement Techniques 6 (11) : 3211-3224. ScholarBank@NUS Repository. https://doi.org/10.5194/amt-6-3211-2013 | |
dc.identifier.issn | 18671381 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/183191 | |
dc.description.abstract | This paper demonstrates the capabilities of chemical ionization mass spectrometry (CIMS) to study secondary organic aerosol (SOA) composition with a high-resolution (HR) time-of-flight mass analyzer (aerosol-ToF-CIMS). In particular, by studying aqueous oxidation of water-soluble organic compounds (WSOC) extracted from ?-pinene ozonolysis SOA, we assess the capabilities of three common CIMS reagent ions: (a) protonated water clusters (H 2O)nH+, (b) acetate CH3C(O)O- and (c) iodide water clusters I(H2O)n- to monitor SOA composition. Furthermore, we report the relative sensitivity of these reagent ions to a wide range of common organic aerosol constituents. We find that (H2O)nH+ is more selective to the detection of less oxidized species, so that the range of O / C and OSC (carbon oxidation state) in the SOA spectra is considerably lower than those measured using CH3C(O)O- and I(H2O)n - Specifically, (H2O)nH+ ionizes organic compounds with OSC ≤ 1.3, whereas CH3C(O)O- and I(H 2O)n- both ionize highly oxygenated organics with OSC up to 4 with I(H2O)n- being more selective towards multi-functional organic compounds. In the bulk O / C and H / C space (in a Van Krevelen plot), there is a remarkable agreement in both absolute magnitude and oxidation trajectory between ToF-CIMS data and those from a high-resolution aerosol mass spectrometer (HR-AMS). Despite not using a sensitivity-weighted response for the ToF-CIMS data, the CIMS approach appears to capture much of the chemical change occurring. As demonstrated by the calibration experiments with standards, this is likely because there is not a large variability in sensitivities from one highly oxygenated species to another, particularly for the CH3- and I(H2O)n- reagent ions. Finally, the data illustrate the capability of aerosol-ToF-CIMS to monitor specific chemical change, including the fragmentation and functionalization reactions that occur during organic oxidation, and the oxidative conversion of dimeric SOA species into monomers. Overall, aerosol-ToF-CIMS is a valuable, selective complement to some common SOA characterization methods, such as AMS and spectroscopic techniques. Both laboratory and ambient SOA samples can be analyzed using the techniques illustrated in the paper. © 2013 Author(s).f 0. | |
dc.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20201031 | |
dc.subject | aerosol composition | |
dc.subject | data set | |
dc.subject | detection method | |
dc.subject | mass spectrometry | |
dc.subject | oxidation | |
dc.subject | ozone | |
dc.type | Article | |
dc.contributor.department | CIVIL AND ENVIRONMENTAL ENGINEERING | |
dc.description.doi | 10.5194/amt-6-3211-2013 | |
dc.description.sourcetitle | Atmospheric Measurement Techniques | |
dc.description.volume | 6 | |
dc.description.issue | 11 | |
dc.description.page | 3211-3224 | |
Appears in Collections: | Staff Publications Elements |
Show simple item record
Files in This Item:
File | Description | Size | Format | Access Settings | Version | |
---|---|---|---|---|---|---|
10_5194_amt-6-3211-2013.pdf | 5.35 MB | Adobe PDF | OPEN | None | View/Download |
This item is licensed under a Creative Commons License