Hydrogen Peroxide Emission and Fate Indoors during Non-bleach Cleaning: A Chamber and Modeling Study

过氧化氢 漂白剂 化学 体积热力学 反应速率常数 环境化学 混合(物理) 臭氧 过氧化物 混合比 环境科学 环境工程 分析化学(期刊) 动力学 有机化学 物理 物理化学 量子力学
作者
Shan Zhou,Zhenlei Liu,Zixu Wang,Cora J. Young,Trevor C. VandenBoer,Bing Guo,Jianshun Zhang,Nicola Carslaw,Tara F. Kahan
出处
期刊:Environmental Science & Technology [American Chemical Society]
卷期号:54 (24): 15643-15651 被引量:31
标识
DOI:10.1021/acs.est.0c04702
摘要

Activities such as household cleaning can greatly alter the composition of air in indoor environments. We continuously monitored hydrogen peroxide (H2O2) from household non-bleach surface cleaning in a chamber designed to simulate a residential room. Mixing ratios of up to 610 ppbv gaseous H2O2 were observed following cleaning, orders of magnitude higher than background levels (sub-ppbv). Gaseous H2O2 levels decreased rapidly and irreversibly, with removal rate constants (kH2O2) 17–73 times larger than air change rate (ACR). Increasing the surface-area-to-volume ratio within the room caused peak H2O2 mixing ratios to decrease and kH2O2 to increase, suggesting that surface uptake dominated H2O2 loss. Volatile organic compound (VOC) levels increased rapidly after cleaning and then decreased with removal rate constants 1.2–7.2 times larger than ACR, indicating loss due to surface partitioning and/or chemical reactions. We predicted photochemical radical production rates and steady-state concentrations in the simulated room using a detailed chemical model for indoor air (the INDCM). Model results suggest that, following cleaning, H2O2 photolysis increased OH concentrations by 10–40% to 9.7 × 105 molec cm–3 and hydroperoxy radical (HO2) concentrations by 50–70% to 2.3 × 107 molec cm–3 depending on the cleaning method and lighting conditions.
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