Formation of secondary organic aerosols from the ozonolysis of dihydrofurans
In this work we report the study of the ozonolysis of 2,5-dihydrofuran and 2,3-dihydrofuran and the reaction conditions leading to the formation of secondary organic aerosols. The reactions have been carried out in a Teflon chamber filled with synthetic air mixtures at atmospheric pressure and room...
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I19-R120-10915-871382024-08-15T18:54:47Z http://sedici.unlp.edu.ar/handle/10915/87138 Formation of secondary organic aerosols from the ozonolysis of dihydrofurans Diaz de Mera, Yolanda Aranda, Alfonso Bracco, Larisa Laura Beatriz Rodríguez, Diana Rodríguez, Ana 2017 2019-12-10T15:15:16Z en Química Aerosoles Ozone Atmospheric conditions In this work we report the study of the ozonolysis of 2,5-dihydrofuran and 2,3-dihydrofuran and the reaction conditions leading to the formation of secondary organic aerosols. The reactions have been carried out in a Teflon chamber filled with synthetic air mixtures at atmospheric pressure and room temperature. The ozonolysis only produced particles in the presence of SO2. Rising relative humidity from 0 to 40% had no effect on the production of secondary organic aerosol in the case of 2,5-dihydrofuran, while it reduced the particle number and particle mass concentrations from the 2,3-dihydrofuran ozonolysis. The water-to-SO2 rate constant ratio for the 2,3-dihydrofuran Criegee intermediate was derived from the secondary organic aerosol (SOA) yields in experiments with different relative humidity values, kH2O/kSO2 = (9.8 ± 3.7) × 10-5. The experimental results show that SO3 may not be the only intermediate involved in the formation or growth of new particles in contrast to the data reported for other Criegee intermediate-SO2 reactions. For the studied reactions, SO2 concentrations remained constant during the experiments, behaving as a catalyst in the production of condensable products. Computational calculations also show that the stabilised Criegee intermediates from the ozonolysis reaction of both 2,5-dihydrofuran and 2,3-dihydrofuran may react with SO2, resulting in the regeneration of SO2 and the formation of low-volatility organic acids. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas Articulo Articulo http://creativecommons.org/licenses/by/3.0/ Creative Commons Attribution 3.0 Unported (CC BY 3.0) application/pdf 2347-2357 |
institution |
Universidad Nacional de La Plata |
institution_str |
I-19 |
repository_str |
R-120 |
collection |
SEDICI (UNLP) |
language |
Inglés |
topic |
Química Aerosoles Ozone Atmospheric conditions |
spellingShingle |
Química Aerosoles Ozone Atmospheric conditions Diaz de Mera, Yolanda Aranda, Alfonso Bracco, Larisa Laura Beatriz Rodríguez, Diana Rodríguez, Ana Formation of secondary organic aerosols from the ozonolysis of dihydrofurans |
topic_facet |
Química Aerosoles Ozone Atmospheric conditions |
description |
In this work we report the study of the ozonolysis of 2,5-dihydrofuran and 2,3-dihydrofuran and the reaction conditions leading to the formation of secondary organic aerosols. The reactions have been carried out in a Teflon chamber filled with synthetic air mixtures at atmospheric pressure and room temperature. The ozonolysis only produced particles in the presence of SO2. Rising relative humidity from 0 to 40% had no effect on the production of secondary organic aerosol in the case of 2,5-dihydrofuran, while it reduced the particle number and particle mass concentrations from the 2,3-dihydrofuran ozonolysis. The water-to-SO2 rate constant ratio for the 2,3-dihydrofuran Criegee intermediate was derived from the secondary organic aerosol (SOA) yields in experiments with different relative humidity values, kH2O/kSO2 = (9.8 ± 3.7) × 10-5. The experimental results show that SO3 may not be the only intermediate involved in the formation or growth of new particles in contrast to the data reported for other Criegee intermediate-SO2 reactions. For the studied reactions, SO2 concentrations remained constant during the experiments, behaving as a catalyst in the production of condensable products. Computational calculations also show that the stabilised Criegee intermediates from the ozonolysis reaction of both 2,5-dihydrofuran and 2,3-dihydrofuran may react with SO2, resulting in the regeneration of SO2 and the formation of low-volatility organic acids. |
format |
Articulo Articulo |
author |
Diaz de Mera, Yolanda Aranda, Alfonso Bracco, Larisa Laura Beatriz Rodríguez, Diana Rodríguez, Ana |
author_facet |
Diaz de Mera, Yolanda Aranda, Alfonso Bracco, Larisa Laura Beatriz Rodríguez, Diana Rodríguez, Ana |
author_sort |
Diaz de Mera, Yolanda |
title |
Formation of secondary organic aerosols from the ozonolysis of dihydrofurans |
title_short |
Formation of secondary organic aerosols from the ozonolysis of dihydrofurans |
title_full |
Formation of secondary organic aerosols from the ozonolysis of dihydrofurans |
title_fullStr |
Formation of secondary organic aerosols from the ozonolysis of dihydrofurans |
title_full_unstemmed |
Formation of secondary organic aerosols from the ozonolysis of dihydrofurans |
title_sort |
formation of secondary organic aerosols from the ozonolysis of dihydrofurans |
publishDate |
2017 |
url |
http://sedici.unlp.edu.ar/handle/10915/87138 |
work_keys_str_mv |
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1809234678967697408 |