Observations of Secondary Organic Aerosol Production and Soot Aging Under Atmospheric Conditions Using a Novel Environmental Aerosol Chamber

Observations of Secondary Organic Aerosol Production and Soot Aging Under Atmospheric Conditions Using a Novel Environmental Aerosol Chamber
Author: Crystal Glen
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Total Pages:
Release: 2012
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Secondary organic aerosols (SOA) comprise a substantial fraction of the total global aerosol budget. While laboratory studies involving smog chambers have advanced our understanding of the formation mechanisms responsible for SOA, our knowledge of the processes leading to SOA production under ambient gaseous and particulate concentrations as well as the impact these aerosol types have on climate is poorly understood. Although the majority of atmospheric aerosols scatter radiation either directly or indirectly by serving as cloud condensation nuclei, soot is thought to have a significant warming effect through absorption. Like inorganic salts, soot may undergo atmospheric transformation through the vapor condensation of non-volatile gaseous species which will alter both its chemical and physical properties. Typical smog chamber studies investigating the formation and growth of SOA as well as the soot aging process are temporally limited by the initial gaseous concentrations injected into the chamber environment. Furthermore, data interpretation from such experiments is generally restricted to the singular gaseous species under investigation. This dissertation discusses the use of a new aerosol chamber designed to study the formation and growth of SOA and soot aging under atmospherically relevant conditions. The Ambient Aerosol Chamber for Evolution Studies (AACES) was deployed at three field sites where size and hygroscopic growth factor (HGF) of ammonium sulfate seed particles was monitored over time to examine the formation and growth of SOA. Similar studies investigating the soot aging process were also conducted in Houston, TX. It is shown that during the ambient growth of ammonium sulfate seed particles, as particle size increases, hygroscopic growth factors decrease considerably resulting in a significant organic mass fraction in the particle phase concluding an experiment. Observations of soot aging show an increase in measured size, HGF, mass and single scattering albedo. Ambient growth rate comparisons with chamber growth yielded similar trends verifying the use of AACES to study aerosol aging. Based on the results from this study, it is recommended that AACES be employed in future studies involving the production and growth of SOA and soot aging under ambient conditions in order to bridge the gaps in our current scientific knowledge.


Observations of Secondary Organic Aerosol Production and Soot Aging Under Atmospheric Conditions Using a Novel Environmental Aerosol Chamber
Language: en
Pages:
Authors: Crystal Glen
Categories:
Type: BOOK - Published: 2012 - Publisher:

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Secondary organic aerosols (SOA) comprise a substantial fraction of the total global aerosol budget. While laboratory studies involving smog chambers have advan
The Aging of Organic Aerosol in the Atmosphere
Language: en
Pages: 134
Authors: Sean Herbert Kessler
Categories:
Type: BOOK - Published: 2013 - Publisher:

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The immense chemical complexity of atmospheric organic particulate matter ("aerosol") has left the general field of condensed-phase atmospheric organic chemistr
Investigation of Fundamental Processes Governing Secondary Organic Aerosol Formation in Laboratory Chambers
Language: en
Pages: 0
Authors: Xuan Zhang
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Type: BOOK - Published: 2015 - Publisher:

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Our understanding of the processes and mechanisms by which secondary organic aerosol (SOA) is formed is derived from laboratory chamber studies. In the atmosphe
Atmospheric Aerosol Aging Involving Organic Compounds and Impacts on Particle Properties
Language: en
Pages:
Authors: Chong Qiu
Categories:
Type: BOOK - Published: 2013 - Publisher:

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In the first part of this dissertation, we study the aging of soot, a representative type of primary aerosols, in the presence of OH-initiated oxidation product