Mechanistic study of secondary organic aerosol components formed from nucleophilic addition reactions of methacrylic acid epoxide
Abstract
Recently, methacrylic acid epoxide (MAE) has been proposed as a precursor to an important class of isoprene-derived compounds found in secondary organic aerosol (SOA): 2-methylglyceric acid (2-MG) and a set of oligomers, nitric acid esters, and sulfuric acid esters related to 2-MG. However, the specific chemical mechanisms by which MAE could form these compounds have not been previously studied with experimental methods. In order to determine the relevance of these processes to atmospheric aerosol, MAE and 2-MG have been synthesized and a series of bulk solution-phase experiments aimed at studying the reactivity of MAE using nuclear magnetic resonance (NMR) spectroscopy have been performed. The present results indicate that the acid-catalyzed MAE reaction is more than 600 times slower than a similar reaction of an important isoprene-derived epoxide, but is still expected to be kinetically feasible in the atmosphere on more acidic SOA. The specific mechanism by which MAE leads to oligomers was identified, and the reactions of MAE with a number of atmospherically relevant nucleophiles were also investigated. Because the nucleophilic strengths of water, sulfate, alcohols (including 2-MG), and acids (including MAE and 2-MG) in their reactions with MAE were found to be of similar magnitudes, it is expected that a diverse variety of MAE + nucleophile product species may be formed on ambient SOA. Thus, the results indicate that epoxide chain reaction oligomerization will be limited by the presence of high concentrations of non-epoxide nucleophiles (such as water); this finding is consistent with previous environmental chamber investigations of the relative humidity dependence of 2-MG-derived oligomerization processes and suggests that extensive oligomerization may not be likely on ambient SOA because of other competitive MAE reaction mechanisms.
Repository Citation
Birdsall, A.W., C.R. Miner, L.E. Mael, and M.J. Elrod. 2014. "Mechanistic study of secondary organic aerosol components formed from nucleophilic addition reactions of methacrylic acid epoxide." Atmospheric Chemistry and Physics 14: 12951-12964.
Publisher
European Geosciences Union / Copernicus Publications
Publication Date
1-1-2014
Publication Title
Atmospheric Chemistry and Physics
Department
Chemistry and Biochemistry
Document Type
Article
DOI
https://dx.doi.org/10.5194/acp-14-12951-2014
Keywords
Isoprene-derived organosulfates, Flight mass-spectrometry, 2-methylglyceric acid, Ambient aerosol, United States, SOA formation, Photooxidation, Kinetics, Hydrolysis, Epoxydiols
Language
English
Format
text