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Science for Society Buildings account for a significant fraction of the land area in cities and actively exchange air with their proximate outdoor environments via mechanical ventilation systems. However, the direct impact of buildings on urban air pollution remains poorly characterized. Due to reductions in traffic-associated emissions of volatile organic compounds (VOCs), volatile chemical products, which are widely used inside buildings, have become a major VOC source in urban areas. Indoor-generated VOCs are likely to be an important contributor to the VOC burden of the urban atmosphere, and ventilation systems provide a pathway for VOCs to be released outdoors. Here, we show how modern buildings act as significant emission sources of VOCs for the outdoor environment. Our results demonstrate that future air quality monitoring efforts in cities need to account for direct VOC discharge from buildings in order to capture emerging sources of environmental pollution that can impact the climate and human health. Summary Urban air undergoes transformations as it is actively circulated throughout buildings via ventilation systems. However, the influence of air exchange between outdoor and indoor atmospheres on urban air pollution is not well understood. Here, we quantify how buildings behave as a dynamic source and sink for urban air pollutants via high-resolution online mass spectrometry measurements. During our field campaign in a high-performance office building, we observed that the building continually released volatile organic compounds (VOCs) into the urban air and removed outdoor ozone and fine particulate matter. VOC emissions from people, their activities, and surface reservoirs result in significant VOC discharge from the building to the outdoors. Per unit area, building emissions of VOCs are comparable to traffic, industrial, and biogenic emissions. The building source-sink behavior changed dynamically with occupancy and ventilation conditions. Our results demonstrate that buildings can directly influence urban air quality due to substantial outdoor-indoor air exchange. 

Scented wax products, such as candles and wax warmers/melts, are popular fragranced consumer products that are commonly used in residential buildings. As scented wax products are intentionally fragranced to produce pleasant smellscapes for occupants, they may represent an important source of volatile organic compounds (VOCs) to indoor atmospheres. The aim of this study is to evaluate terpene emission factors (EFs) and inhalation intake fractions (iFs) for scented wax products to better understand their impact on indoor chemistry and chemical exposures. Full-scale emission experiments were conducted in the Purdue zEDGE Test House using a variety of scented candles (n = 5) and wax warmers/melts (n = 14) under different outdoor air exchange rates (AERs). Terpene concentrations were measured in real-time using a proton transfer reaction time-of-flight mass spectrometer (PTR-TOF-MS). PTR-TOF-MS measurements revealed that scented candle and wax warmer/melt products emit a variety of monoterpenes (C10H16) and oxygen-containing monoterpenoids (C10H14O, C10H16O, C10H18O, C10H20O), with peak concentrations in the range of 10^−1 to 10^2 ppb. Monoterpene EFs were much greater for scented wax warmers/melts (C10H16 EFs ~ 10^2 mg per g wax consumed) compared to scented candles (C10H16 EFs ~ 10^−1 to 100 mg per g wax consumed). Significant emissions of reactive terpenes from both products, along with nitrogen oxides (NO, NO2) from candles, depleted indoor ozone (O3) concentrations. Terpene iFs were similar between the two products (iFs ~ 10^3 ppm) and increased with decreasing outdoor AER. Terpene iFs during concentration decay periods were similar to, or greater than, iFs during active emission periods for outdoor AERs ≤ 3.0 h^−1. Overall, scented wax warmers/melts were found to release greater quantities of monoterpenes compared to other fragranced consumer products used in the home, including botanical disinfectants, hair care products, air fresheners, and scented sprays. 

Cyclic volatile methyl siloxanes (cVMS) are ubiquitous in hair care products (HCPs). cVMS emissions from HCPs are of concern, given the potential adverse impact of siloxanes on the environment and human health. To characterize cVMS emissions and exposures during the use of HCPs, realistic hair care experiments were conducted in a residential building. Siloxane-based HCPs were tested using common hair styling techniques, including straightening, curling, waving, and oiling. VOC concentrations were measured via proton-transfer-reaction time-of-flight mass spectrometry. HCP use drove rapid changes in the chemical composition of the indoor atmosphere. cVMS dominated VOC emissions from HCP use, and decamethylcyclopentasiloxane (D5) contributed the most to cVMS emissions. cVMS emission factors (EFs) during hair care routines ranged from 110–1500 mg/person and were influenced by HCP type, styling tools, operation temperatures, and hair length. The high temperature of styling tools and the high surface area of hair enhanced VOC emissions. Increasing the hair straightener temperature from room temperature to 210 °C increased cVMS EFs by 50–310%. Elevated indoor cVMS concentrations can result in substantial indoor-to-outdoor transport of cVMS via ventilation (0.4–6 tons D5/year in the U.S.); thus, hair care routines may augment the abundance of cVMS in the outdoor atmosphere.