Journal cover Journal topic
Atmospheric Chemistry and Physics An interactive open-access journal of the European Geosciences Union
Atmos. Chem. Phys., 16, 11563-11580, 2016
https://doi.org/10.5194/acp-16-11563-2016
© Author(s) 2016. This work is distributed under
the Creative Commons Attribution 3.0 License.
Research article
19 Sep 2016
Volatility and lifetime against OH heterogeneous reaction of ambient isoprene-epoxydiols-derived secondary organic aerosol (IEPOX-SOA)
Weiwei Hu1,2, Brett B. Palm1,2, Douglas A. Day1,2, Pedro Campuzano-Jost1,2, Jordan E. Krechmer1,2, Zhe Peng1,2, Suzane S. de Sá3, Scot T. Martin3,4, M. Lizabeth Alexander5, Karsten Baumann6, Lina Hacker7, Astrid Kiendler-Scharr7, Abigail R. Koss1,2,8, Joost A. de Gouw1,2,8, Allen H. Goldstein9,10, Roger Seco11, Steven J. Sjostedt8, Jeong-Hoo Park12, Alex B. Guenther11, Saewung Kim11, Francesco Canonaco13, André S. H. Prévôt13, William H. Brune14, and Jose L. Jimenez1,2 1Cooperative Institute for Research in Environmental Sciences, University of Colorado, Boulder, CO 80309, USA
2Department of Chemistry and Biochemistry, University of Colorado, Boulder, CO 80309, USA
3John A. Paulson School of Engineering and Applied Sciences Harvard University, Cambridge, MA 01742, USA
4Department of Earth and Planetary Sciences, Harvard University, Cambridge, MA 01742, USA
5Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, WA 99352, USA
6Atmospheric Research and Analysis Inc., Morrisville, NC 27560, USA
7Institute for Energy and Climate Research – Troposphere (IEK-8), Forschungszentrum Jülich, 52425 Jülich, Germany
8Earth System Research Laboratory, NOAA, Boulder, CO 80305, USA
9Department of Environmental Science, Policy, and Management, University of California, Berkeley, CA 94720, USA
10Department of Civil and Environmental Engineering, University of California, Berkeley, CA 94720, USA
11Department of Earth System Science, University of California, Irvine, CA 92697, USA
12National Institute of Environmental Research, Incheon 22689, Republic of Korea
13Laboratory of Atmospheric Chemistry, Paul Scherrer Institute (PSI), 5232 Villigen, Switzerland
14Department of Meteorology, Pennsylvania State University, University Park, PA 16802, USA
Abstract. Isoprene-epoxydiols-derived secondary organic aerosol (IEPOX-SOA) can contribute substantially to organic aerosol (OA) concentrations in forested areas under low NO conditions, hence significantly influencing the regional and global OA budgets, accounting, for example, for 16–36 % of the submicron OA in the southeastern United States (SE US) summer. Particle evaporation measurements from a thermodenuder show that the volatility of ambient IEPOX-SOA is lower than that of bulk OA and also much lower than that of known monomer IEPOX-SOA tracer species, indicating that IEPOX-SOA likely exists mostly as oligomers in the aerosol phase. The OH aging process of ambient IEPOX-SOA was investigated with an oxidation flow reactor (OFR). New IEPOX-SOA formation in the reactor was negligible, as the OFR does not accelerate processes such as aerosol uptake and reactions that do not scale with OH. Simulation results indicate that adding  ∼  100 µg m−3 of pure H2SO4 to the ambient air allows IEPOX-SOA to be efficiently formed in the reactor. The heterogeneous reaction rate coefficient of ambient IEPOX-SOA with OH radical (kOH) was estimated as 4.0 ± 2.0  ×  10−13 cm3 molec−1 s−1, which is equivalent to more than a 2-week lifetime. A similar kOH was found for measurements of OH oxidation of ambient Amazon forest air in an OFR. At higher OH exposures in the reactor (>  1  ×  1012 molec cm−3 s), the mass loss of IEPOX-SOA due to heterogeneous reaction was mainly due to revolatilization of fragmented reaction products. We report, for the first time, OH reactive uptake coefficients (γOH =  0.59 ± 0.33 in SE US and γOH =  0.68 ± 0.38 in Amazon) for SOA under ambient conditions. A relative humidity dependence of kOH and γOH was observed, consistent with surface-area-limited OH uptake. No decrease of kOH was observed as OH concentrations increased. These observations of physicochemical properties of IEPOX-SOA can help to constrain OA impact on air quality and climate.

Citation: Hu, W., Palm, B. B., Day, D. A., Campuzano-Jost, P., Krechmer, J. E., Peng, Z., de Sá, S. S., Martin, S. T., Alexander, M. L., Baumann, K., Hacker, L., Kiendler-Scharr, A., Koss, A. R., de Gouw, J. A., Goldstein, A. H., Seco, R., Sjostedt, S. J., Park, J.-H., Guenther, A. B., Kim, S., Canonaco, F., Prévôt, A. S. H., Brune, W. H., and Jimenez, J. L.: Volatility and lifetime against OH heterogeneous reaction of ambient isoprene-epoxydiols-derived secondary organic aerosol (IEPOX-SOA), Atmos. Chem. Phys., 16, 11563-11580, https://doi.org/10.5194/acp-16-11563-2016, 2016.
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Short summary
IEPOX-SOA is biogenically derived secondary organic aerosol under anthropogenic influence, which has been shown to comprise a substantial fraction of OA globally. We investigated the lifetime of ambient IEPOX-SOA in the SE US and Amazonia, with an oxidation flow reactor and thermodenuder coupled with MS-based instrumentation. The low volatility and long lifetime of IEPOX-SOA against OH radicals' oxidation (> 2 weeks) was observed, which can help to constrain OA impact on air quality and climate.
IEPOX-SOA is biogenically derived secondary organic aerosol under anthropogenic influence, which...
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