| Autor: |
Downey JP; Department of Chemistry, University of Toronto, Toronto, Ontario M5S 3H6, Canada., Lakey PSJ; Department of Chemistry, University of California, Irvine, California 92697, United States., Shiraiwa M; Department of Chemistry, University of California, Irvine, California 92697, United States., Abbatt JPD; Department of Chemistry, University of Toronto, Toronto, Ontario M5S 3H6, Canada. |
| Jazyk: |
angličtina |
| Zdroj: |
Environmental science & technology [Environ Sci Technol] 2024 Jul 09; Vol. 58 (27), pp. 12073-12081. Date of Electronic Publication: 2024 Jun 26. |
| DOI: |
10.1021/acs.est.4c02208 |
| Abstrakt: |
Ozone and its oxidation products result in negative health effects when inhaled. Despite painted surfaces being the most abundant surface in indoor spaces, surface loss remains one of the largest uncertainties in the indoor ozone budget. Here, ozone uptake coefficients (γ O3 ) on painted surfaces were measured in a flow-through reactor where 79% of the inner surfaces were removable painted glass sheets. Flat white paint initially had a high uptake coefficient (8.3 × 10 -6 ) at 20% RH which plateaued to 1.1 × 10 -6 as the paint aged in an indoor office over weeks. Increasing the RH from 0 to 75% increased γ O3 by a factor of 3.0, and exposure to 134 ppb of α-terpineol for 1 h increased γ O3 by a factor of 1.6 at 20% RH. RH also increases α-terpineol partitioning to paint, further increasing ozone loss, but the type of paint (flat, eggshell, satin, semigloss) had no significant effect. A kinetic multilayer model captures the dependence of γ O3 on RH and the presence of α-terpineol, indicating the reacto-diffusive depth for O 3 is 1 to 2 μm. Given the similarity of the kinetics on aged surfaces across many paint types and the sustained reactivity during aging, these results suggest a mechanism for catalytic loss. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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