Formation of 9,10-phenanthrenequinone by atmospheric gas-phase reactions of phenanthrene [An article from: Atmospheric Environment]
Book Details
Author(s)L. Wang, R. Atkinson, J. Arey
PublisherElsevier
ISBN / ASINB000PDTDLO
ISBN-13978B000PDTDL2
MarketplaceFrance 🇫🇷
Description
This digital document is a journal article from Atmospheric Environment, published by Elsevier in 2007. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.
Description:
Phenanthrene is a 3-ring polycyclic aromatic hydrocarbon which exists mainly in the gas-phase in the atmosphere. Recent concern over the presence of 9,10-phenanthrenequinone in ambient particles led us to study the products of the gas-phase reactions of phenanthrene with hydroxyl radicals, nitrate radicals and ozone. The formation yields of 9,10-phenanthrenequinone were measured to be ~3%, 33+/-9%, and ~2% from the OH radical, NO"3 radical and O"3 reactions, respectively. Calculations suggest that daytime OH radical-initiated and nighttime NO"3 radical-initiated reactions of gas-phase phenanthrene may be significant sources of 9,10-phenanthrenequinone in ambient atmospheres. In contrast, the ozone reaction with phenanthrene is unlikely to contribute significantly to ambient 9,10-phenanthrenequinone.
Description:
Phenanthrene is a 3-ring polycyclic aromatic hydrocarbon which exists mainly in the gas-phase in the atmosphere. Recent concern over the presence of 9,10-phenanthrenequinone in ambient particles led us to study the products of the gas-phase reactions of phenanthrene with hydroxyl radicals, nitrate radicals and ozone. The formation yields of 9,10-phenanthrenequinone were measured to be ~3%, 33+/-9%, and ~2% from the OH radical, NO"3 radical and O"3 reactions, respectively. Calculations suggest that daytime OH radical-initiated and nighttime NO"3 radical-initiated reactions of gas-phase phenanthrene may be significant sources of 9,10-phenanthrenequinone in ambient atmospheres. In contrast, the ozone reaction with phenanthrene is unlikely to contribute significantly to ambient 9,10-phenanthrenequinone.
