Rate and Reaction Probability of the Surface Reaction between Ozone and Dihydromyrcenol Measured in a Bench Scale Reactor and a Room-sized Chamber
Abstract
Low volatility terpenoids emitted from consumer products can react with ozone on surfaces and may significantly alter concentrations of ozone, terpenoids and reaction products in indoor air. We measured the reaction probability and a second-order surface-specific reaction rate for the ozonation of dihydromyrcenol, a representative indoor terpenoid, adsorbed onto polyvinylchloride (PVC), glass, and latex paint coated spheres. the reaction probability ranged from (0.06-8.97)-x-10 -5 and was very sensitive to humidity, substrate and mass adsorbed. the average surface reaction probability is about 10 times greater than that for the gas-phase reaction. the second-order surface-specific rate coefficient ranged from (0.32-7.05)-x-10 -15-cm 4-s -1-molecule -1and was much less sensitive to humidity, substrate, or mass adsorbed. We also measured the ozone deposition velocity due to adsorbed dihydromyrcenol on painted drywall in a room-sized chamber, based on that, we calculated the rate coefficient ((0.42-1.6)-x-10 -15-cm 4-molecule -1-s -1), which was consistent with that derived from bench-scale experiments for the latex paint under similar conditions. We predict that more than 95% of dihydromyrcenol oxidation takes place on indoor surfaces, rather than in building air. © 2011 Elsevier Ltd.
Recommended Citation
S. Shu and G. C. Morrison, "Rate and Reaction Probability of the Surface Reaction between Ozone and Dihydromyrcenol Measured in a Bench Scale Reactor and a Room-sized Chamber," Atmospheric Environment, vol. 47, pp. 421 - 427, Elsevier, Feb 2012.
The definitive version is available at https://doi.org/10.1016/j.atmosenv.2011.10.068
Department(s)
Civil, Architectural and Environmental Engineering
Keywords and Phrases
Dihydromyrcenol; Indoor air; Kinetics; Ozone; Surface reactions
International Standard Serial Number (ISSN)
1873-2844; 1352-2310
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2024 Elsevier, All rights reserved.
Publication Date
01 Feb 2012
Comments
National Science Foundation, Grant 0238721