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Chemical composition of isoprene SOA under acidic and non-acidic conditions: effect of relative humidity
The effect of acidity and relative humidity on bulk isoprene aerosol parameters has been investigated in several studies; however, few measurements have been conducted on individual aerosol compounds. The focus of this study has been the examination of the effect of acidity and relative humidity on...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7063744/ https://www.ncbi.nlm.nih.gov/pubmed/32158471 http://dx.doi.org/10.5194/acp-18-18101-2018 |
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author | Nestorowicz, Klara Jaoui, Mohammed Rudzinski, Krzysztof Jan Lewandowski, Michael Kleindienst, Tadeusz E. Spólnik, Grzegorz Danikiewicz, Witold Szmigielski, Rafal |
author_facet | Nestorowicz, Klara Jaoui, Mohammed Rudzinski, Krzysztof Jan Lewandowski, Michael Kleindienst, Tadeusz E. Spólnik, Grzegorz Danikiewicz, Witold Szmigielski, Rafal |
author_sort | Nestorowicz, Klara |
collection | PubMed |
description | The effect of acidity and relative humidity on bulk isoprene aerosol parameters has been investigated in several studies; however, few measurements have been conducted on individual aerosol compounds. The focus of this study has been the examination of the effect of acidity and relative humidity on secondary organic aerosol (SOA) chemical composition from isoprene photooxidation in the presence of nitrogen oxide (NO(x)). A detailed characterization of SOA at the molecular level was also investigated. Experiments were conducted in a 14.5 m(3) smog chamber operated in flow mode. Based on a detailed analysis of mass spectra obtained from gas chromatography–mass spectrometry of silylated derivatives in electron impact and chemical ionization modes, ultra-high performance liquid chromatography/electrospray ionization/time-of-flight high-resolution mass spectrometry, and collision-induced dissociation in the negative ionization modes, we characterized not only typical isoprene products but also new oxygenated compounds. A series of nitroxy-organosulfates (NOSs) were tentatively identified on the basis of high-resolution mass spectra. Under acidic conditions, the major identified compounds include 2-methyltetrols (2MT), 2-methylglyceric acid (2mGA), and 2MT-OS. Other products identified include epoxydiols, mono- and dicarboxylic acids, other organic sulfates, and nitroxy- and nitrosoxy-OS. The contribution of SOA products from isoprene oxidation to PM(2.5) was investigated by analyzing ambient aerosol collected at rural sites in Poland. Methyltetrols, 2mGA, and several organosulfates and nitroxy-OS were detected in both the field and laboratory samples. The influence of relative humidity on SOA formation was modest in non-acidic-seed experiments and stronger under acidic seed aerosol. Total secondary organic carbon decreased with increasing relative humidity under both acidic and non-acidic conditions. While the yields of some of the specific organic compounds decreased with increasing relative humidity, others varied in an indeterminate manner from changes in the relative humidity. |
format | Online Article Text |
id | pubmed-7063744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-70637442020-03-10 Chemical composition of isoprene SOA under acidic and non-acidic conditions: effect of relative humidity Nestorowicz, Klara Jaoui, Mohammed Rudzinski, Krzysztof Jan Lewandowski, Michael Kleindienst, Tadeusz E. Spólnik, Grzegorz Danikiewicz, Witold Szmigielski, Rafal Atmos Chem Phys Article The effect of acidity and relative humidity on bulk isoprene aerosol parameters has been investigated in several studies; however, few measurements have been conducted on individual aerosol compounds. The focus of this study has been the examination of the effect of acidity and relative humidity on secondary organic aerosol (SOA) chemical composition from isoprene photooxidation in the presence of nitrogen oxide (NO(x)). A detailed characterization of SOA at the molecular level was also investigated. Experiments were conducted in a 14.5 m(3) smog chamber operated in flow mode. Based on a detailed analysis of mass spectra obtained from gas chromatography–mass spectrometry of silylated derivatives in electron impact and chemical ionization modes, ultra-high performance liquid chromatography/electrospray ionization/time-of-flight high-resolution mass spectrometry, and collision-induced dissociation in the negative ionization modes, we characterized not only typical isoprene products but also new oxygenated compounds. A series of nitroxy-organosulfates (NOSs) were tentatively identified on the basis of high-resolution mass spectra. Under acidic conditions, the major identified compounds include 2-methyltetrols (2MT), 2-methylglyceric acid (2mGA), and 2MT-OS. Other products identified include epoxydiols, mono- and dicarboxylic acids, other organic sulfates, and nitroxy- and nitrosoxy-OS. The contribution of SOA products from isoprene oxidation to PM(2.5) was investigated by analyzing ambient aerosol collected at rural sites in Poland. Methyltetrols, 2mGA, and several organosulfates and nitroxy-OS were detected in both the field and laboratory samples. The influence of relative humidity on SOA formation was modest in non-acidic-seed experiments and stronger under acidic seed aerosol. Total secondary organic carbon decreased with increasing relative humidity under both acidic and non-acidic conditions. While the yields of some of the specific organic compounds decreased with increasing relative humidity, others varied in an indeterminate manner from changes in the relative humidity. 2018-12-20 /pmc/articles/PMC7063744/ /pubmed/32158471 http://dx.doi.org/10.5194/acp-18-18101-2018 Text en http://creativecommons.org/licenses/by/4.0/ This work is distributed under the Creative Commons Attribution 4.0 License. |
spellingShingle | Article Nestorowicz, Klara Jaoui, Mohammed Rudzinski, Krzysztof Jan Lewandowski, Michael Kleindienst, Tadeusz E. Spólnik, Grzegorz Danikiewicz, Witold Szmigielski, Rafal Chemical composition of isoprene SOA under acidic and non-acidic conditions: effect of relative humidity |
title | Chemical composition of isoprene SOA under acidic and non-acidic conditions: effect of relative humidity |
title_full | Chemical composition of isoprene SOA under acidic and non-acidic conditions: effect of relative humidity |
title_fullStr | Chemical composition of isoprene SOA under acidic and non-acidic conditions: effect of relative humidity |
title_full_unstemmed | Chemical composition of isoprene SOA under acidic and non-acidic conditions: effect of relative humidity |
title_short | Chemical composition of isoprene SOA under acidic and non-acidic conditions: effect of relative humidity |
title_sort | chemical composition of isoprene soa under acidic and non-acidic conditions: effect of relative humidity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7063744/ https://www.ncbi.nlm.nih.gov/pubmed/32158471 http://dx.doi.org/10.5194/acp-18-18101-2018 |
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