|Title||Secondary organic aerosol from ozone-initiated reactions with terpene-rich household products|
|Publication Type||Journal Article|
|Year of Publication||2008|
|Authors||Beverly K Coleman, Melissa M Lunden, Hugo Destaillats, William W Nazaroff|
|Keywords||aerosols, cleaning products, condensation, environmental chemistry, exposure & risk group, indoor air quality, indoor and outdoor, indoor environment department, limonene, nucleation, ozone, secondary organic aerosol, size distribution, terpenes|
We analyzed secondary organic aerosol (SOA) data from a series of small-chamber experiments in which terpene-rich vapors from household products were combined with ozone under conditions analogous to product use indoors. Reagents were introduced into a continuously ventilated 198 L chamber at steady rates. Consistently, at the time of ozone introduction, nucleation occurred exhibiting similar behavior to atmospheric events. The initial nucleation burst and growth was followed by a period in which approximately stable particle levels were established, reflecting a balance between new particle formation, condensational growth, and removal by ventilation. Airborne particles were measured with a scanning mobility particle sizer (SMPS, 10–400 nm) in every experiment and with an optical particle counter (OPC, 0.1–2.0 μm) in a subset. Parameters for a three-mode lognormal fit to the size distribution at steady state were determined for each experiment. Increasing the supply ozone level increased the steady-state mass concentration and yield of SOA from each product tested. Decreasing the air-exchange rate increased the yield. The steady-state fine-particle mass concentration (PM1.1) ranged from 10 to >300 μg m−3 and yields ranged from 5% to 37%. Steady-state nucleation rates and SOA mass formation rates were ∼10 cm−3 s−1 and ∼10 μg m−3 min−1, respectively.