Atmospheric Chemistry of Volatile Organic Compounds: Kinetics, Degradation Mechanisms, and Secondary Organic Aerosols

A special issue of Atmosphere (ISSN 2073-4433). This special issue belongs to the section "Aerosols".

Deadline for manuscript submissions: closed (15 July 2023) | Viewed by 3178

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Faculty of Chemistry and Integrated Centre of Environmental Science Studies in the North Eastern Region (CERNESIM), “Alexandru Ioan Cuza” University of Iasi, 700506 Iasi, Romania
Interests: atmospheric chemistry; photochemistry; physical chemistry; gas phase kinetics; chemical degradation mechanism; aerosols
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Special Issue Information

Dear Colleagues,

Atmospheric chemistry and related topics have been attracting continuous interest over the last few decades. Climate variability and changes have impacted the lifecycles, unbalancing the concentration of the constituents of the Earth’s atmosphere. The budget of gases and particles in the atmosphere is strongly affected by these modifications, further influencing atmospheric processes. The reactivity, composition, and dynamics of trace gases in the atmosphere have challenged our understanding of the chemistry and physics of atmospheric processes. Biogenic and anthropogenic sources of volatile organic compounds are more complex than decades ago, intriguing scientists.

With this Special Issue, we invite you to submit your scientific research articles, which cover a broad range of topics on chemistry and physics of atmosphere from gas-phase reactivity and degradation mechanism to secondary organic aerosol formation. Your contributions may include recent experimental work and modeling studies. The topics of interest are around the aim to better understand atmospheric processes but are not limited to:

  • Ozone, OH and NO3 radicals, and chlorine atoms gas-phase kinetics;
  • Investigations on the relevant atmospheric photochemical processes;
  • Structure–activity relationship and reactivity studies;
  • Gas-phase mechanistic investigations of chemical reactions;
  • VOC chemical degradation and product formation;
  • Modeling applications of reaction kinetics and mechanisms;
  • Formation of secondary organic aerosols from gas phase reactions of VOCs—size distribution, formation yield, and modeling studies;
  • Theoretical and/or computational methodology of atmospheric general interest.

Dr. Iustinian Gabriel Bejan
Guest Editor

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Keywords

  • atmospheric chemistry
  • secondary organic aerosol
  • solar radiation
  • chemical reaction mechanisms
  • photochemistry
  • physical chemistry
  • gas-phase kinetics
  • gas-phase reaction products
  • chemical degradation
  • chemical reactivity
  • aerosol composition
  • biogenic and anthropogenic VOCs

Published Papers (1 paper)

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Research

19 pages, 4025 KiB  
Article
Experimental and Theoretical Studies of Trans-2-Pentenal Atmospheric Ozonolysis
by Carmen Kalalian, Asma Grira, Jan Niklas Illmann, Iulia Patroescu-Klotz, Gisèle El Dib, Patrice Coddeville, André Canosa, Peter Wiesen, Basheer Aazaad, Lakshmipathi Senthilkumar, Estelle Roth, Alexandre Tomas and Abdelkhaleq Chakir
Atmosphere 2022, 13(2), 291; https://doi.org/10.3390/atmos13020291 - 9 Feb 2022
Cited by 2 | Viewed by 2340
Abstract
We investigated the kinetics, mechanism and secondary organic aerosols formation of the ozonolysis of trans-2-pentenal (T2P) using four different reactors with Fourier Transform InfraRed (FTIR) spectroscopy and Gas Chromatography (GC) techniques at T = 298 ± 2 K and 760 Torr in dry [...] Read more.
We investigated the kinetics, mechanism and secondary organic aerosols formation of the ozonolysis of trans-2-pentenal (T2P) using four different reactors with Fourier Transform InfraRed (FTIR) spectroscopy and Gas Chromatography (GC) techniques at T = 298 ± 2 K and 760 Torr in dry conditions. The rate coefficients and branching ratios were also evaluated using the canonical variational transition (CVT) state theory coupled with small curvature tunneling (CVT/SCT) in the range 278–350 K. The experimental rate coefficient at 298 K was (1.46 ± 0.17) × 10−18 cm3 molecule−1 s−1, in good agreement with the theoretical rate. The two primary carbonyls formation yields, glyoxal and propanal, were 57 ± 10% and 42 ± 12%, respectively, with OH scavenger compared to 38 ± 8% for glyoxal and 26 ± 5% for propanal without OH scavenger. Acetaldehyde and 2-hydroxypropanal were also identified and quantified with yields of 9 ± 3% and 5 ± 2%, respectively, in the presence of OH scavenger. For the OH production, an upper limit of 24% was estimated using mesitylene as OH tracer. Combining experimental and theoretical findings enabled the establishment of a chemical mechanism. Finally, the SOA formation was observed with mass yields of about 1.5%. This work provides additional information on the effect of the aldehyde functional group on the fragmentation of the primary ozonide. Full article
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