Abstract
Reactive oxygen species (ROS) are an important contributor to adverse health effects associated with ambient air pollution. Despite infiltration of ROS from outdoors, and possible indoor sources (eg, combustion), there are limited data available on indoor ROS. In this study, part of the second phase of Air Composition and Reactivity from Outdoor aNd Indoor Mixing campaign (ACRONIM-2), we constructed and deployed an online, continuous, system to measure extracellular gas- and particle-phase ROS during summer in an unoccupied residence in St. Louis, MO, USA. Over a period of one week, we observed that the non-denuded outdoor ROS (representing particle-phase ROS and some gas-phase ROS) concentration ranged from 1 to 4 nmol/m3 (as H2O2). Outdoor concentrations were highest in the afternoon, coincident with peak photochemistry periods. The indoor concentrations of particle-phase ROS were nearly equal to outdoor concentrations, regardless of window-opening status or air exchange rates. The indoor/outdoor ratio of non-denuded ROS (I/OROS) was significantly less than 1 with windows open and even lower with windows closed. Combined, these observations suggest that gas-phase ROS are efficiently removed by interior building surfaces and that there may be an indoor source of particle-phase ROS.
Recommended Citation
A. Eftekhari et al., "Continuous Measurement of Reactive Oxygen Species Inside and Outside of a Residential House during Summer," Indoor Air, vol. 31, no. 4, pp. 1199 - 1216, John Wiley & Sons, Jul 2021.
The definitive version is available at https://doi.org/10.1111/ina.12789
Department(s)
Chemistry
Keywords and Phrases
Detached Home; Field Study; Online Measurement; Ozone; PM; ROS
International Standard Serial Number (ISSN)
0905-6947
Document Type
Article - Journal
Document Version
Final Version
File Type
text
Language(s)
English
Rights
© 2021 John Wiley & Sons, All rights reserved.
Publication Date
01 Jul 2021
Comments
This publication was developed under Assistance Agreement No. 83575101 awarded by the U.S. Environmental Protection Agency. This work was also supported by the Alfred P. Sloan Foundation’s Chemistry of Indoor Environments Program.