Acid-base chemical reaction model for nucleation rates in the polluted atmospheric boundary layer.

Climate models show that particles formed by nucleation can affect cloud cover and, therefore, the earth's radiation budget. Measurements worldwide show that nucleation rates in the atmospheric boundary layer are positively correlated with concentrations of sulfuric acid vapor. However, current nucleation theories do not correctly predict either the observed nucleation rates or their functional dependence on sulfuric acid concentrations. This paper develops an alternative approach for modeling nucleation rates, based on a sequence of acid-base reactions. The model uses empirical estimates of sulfuric acid evaporation rates obtained from new measurements of neutral molecular clusters. The model predicts that nucleation rates equal the sulfuric acid vapor collision rate times a prefactor that is less than unity and that depends on the concentrations of basic gaseous compounds and preexisting particles. Predicted nucleation rates and their dependence on sulfuric acid vapor concentrations are in reasonable agreement with measurements from Mexico City and Atlanta.

Personal and indoor exposure to PM2.5 and polycyclic aromatic hydrocarbons in the southern highlands of Tanzania: a pilot-scale study.

Personal and indoor exposure to PM(2.5) and polycyclic aromatic hydrocarbons (PAHs) were measured in households in the Njombe district of Tanzania. Cooking is conducted indoors in this region due to its high elevation, cool climate, and heavy seasonal rainfall. Kitchens are often poorly ventilated, resulting in high exposures to combustion-related pollutants. Sampling sites were selected to represent typical cooking practices across regional socio-economic divisions. These include the use of open wood fires, charcoal, a mix of charcoal and kerosene, and liquid petroleum gas (LPG) for cooking fuels. PM(2.5) average personal exposure was 14 µg/m(3) (±3, n = 3) for LPG, 88 µg/m(3) (±42, n = 3) for kerosene/charcoal mix, 588 µg/m(3) (±347, n = 3) for charcoal alone, and 1574 µg/m(3) (±287, n = 3) for open wood fires. Total PAH average personal exposures were less than 1 ng/m(3) (±1, n = 3) for LPG, 57 ng/m(3) (±16, n = 3) for kerosene/charcoal mix, 334 ng/m(3) (±57, n = 3) for charcoal alone, and 5040 ng/m(3) (±909, n = 3) for open wood fires. Benzo[a]pyrene equivalent exposures for US EPA's priority PAH pollutants were 0 for LPG, 8 ng/m(3) for kerosene/charcoal mix, 44 ng/m(3) for charcoal, and 767 ng/m(3) for open wood fire. Inhalable pollutants are present at unacceptably high levels, exceeding indoor air quality standards for all but LPG fuels. Relative results provide an exposure profile for rural East Africa and support the feasibility of conducting a larger scale smoke exposure campaign in the region. The use of "fuel efficient" wood stoves for the reduction of PM(2.5) and PAH exposure was measured in a local secondary school. Proper use of "fuel efficient" wood stoves reduced personal and indoor exposure to measured pollutants by more than 90%, supporting further investigation into the applicability of this technology to significantly improve indoor air quality.