Reactions of Hydroxyl Radicals and Ozone with Acenaphthene and Acenaphthylene
Fabienne Reisen, Janet Arey
Abstract
Fabienne Reisen, Janet Arey
Abstract
Acenaphthene and acenaphthylene are polycyclic aromatic hydrocarbons (PAHs) emitted into the atmosphere from a variety of incomplete combustion sources such as diesel exhaust. Both PAHs are present in the gas phase under typical atmospheric conditions and therefore can undergo atmospheric gas-phase reactions with the hydroxyl (OH) radical and for acenaphthylene with ozone. Using a relative rate method, rate constants have been measured at 296 +/- 2 K for the OH radical reactions with acenaphthene and acenaphthylene of (in units of 10(-11) cm3 molecule(-1) s(-1)) 8.0 +/- 0.4 and 12.4 +/- 0.7, respectively, and for the O3 reaction with acenaphthylene of (1.6 +/- 0.1) x 10(-16) cm3 molecule(-1) s(-1). The products of the gas-phase reactions of acenaphthene and acenaphthylene and their fully deuterated analogues have been investigated using in situ atmospheric pressure ionization tandem mass spectrometry (API-MS) and gas chromatography-mass spectrometry (GC-MS). The major products identified from the OH radical-initiated reaction of acenaphthene and acenaphthylene were a 10 carbon ring-opened product and a dialdehyde, respectively. The major product observed from the API-MS analysis of the O3 reaction with acenaphthylene was a secondary ozonide, which was not observed by GC-MS.
OpenAlex reports 85 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Acenaphthene and acenaphthylene are polycyclic aromatic hydrocarbons (PAHs) emitted into the atmosphere from a variety of incomplete combustion sources such as diesel exhaust. Both PAHs are present in the gas phase under typical atmospheric conditions and therefore can undergo atmospheric gas-phase reactions with the hydroxyl (OH) radical and for acenaphthylene with ozone. Using a relative rate method, rate constants have been measured at 296 +/- 2 K for the OH radical reactions with acenaphthene and acenaphthylene of (in units of 10(-11) cm3 molecule(-1) s(-1)) 8.0 +/- 0.4 and 12.4 +/- 0.7, respectively, and for the O3 reaction with acenaphthylene of (1.6 +/- 0.1) x 10(-16) cm3 molecule(-1) s(-1). The products of the gas-phase reactions of acenaphthene and acenaphthylene and their fully deuterated analogues have been investigated using in situ atmospheric pressure ionization tandem mass spectrometry (API-MS) and gas chromatography-mass spectrometry (GC-MS). The major products identified from the OH radical-initiated reaction of acenaphthene and acenaphthylene were a 10 carbon ring-opened product and a dialdehyde, respectively. The major product observed from the API-MS analysis of the O3 reaction with acenaphthylene was a secondary ozonide, which was not observed by GC-MS.
Key concepts: Acenaphthene, Acenaphthylene, Radical, Ozone, Photochemistry, Chemistry, Environmental chemistry, Organic chemistry