Aerosols have significant impacts on earth's climate and hydrological cycle. They can directly reflect the amount of incoming solar radiation into space; by acting as cloud condensation nuclei (CCN), they can indirectly impact climate by affecting cloud albedo. Our current assessment of the interactions of aerosols and clouds is uncertain and parameters used to estimate cloud droplet formation in global climate models are not well constrained. Organic aerosols attribute much of the uncertainty in these estimates and are known to affect the ability of aerosol to form cloud droplets (CCN Activity) by i) providing solute, thus reducing the equilibrium water vapor pressure of the droplet and ii) acting as surfactants capable of depressing surface tension, and potentially, growth kinetics. My thesis dissertation investigates various organic aerosol species (e.g., marine, urban, biomass burning, Humic-like Substances). An emphasis is placed on the water soluble components and secondary organic aerosols (SOA). In addition the sampled organic aerosols are acquired via different media; directly from in-situ ambient studies (TEXAQS 2006) environmental chamber experiments, regenerated from filters, and cloud water samples. Novel experimental methods and analyses to determine surface tension, molar volumes, and droplet growth rates are presented from nominal volumes of sample. These key parameters for cloud droplet formation incorporated into climate models will constrain aerosol-cloud interactions and provide a more accurate assessment for climate prediction.

It is well known that atmospheric aerosols provide the sites for forming cloud droplets, and can affect the Earth's radiation budget through their interactions with clouds. The ability of aerosols to act as cloud condensation nuclei is a strong function of their chemical composition and size. The compositional complexity of aerosol prohibits their explicit treatment in atmospheric models of aerosol-cloud interactions. Nevertheless, the cumulative impact of organics on CCN activity is still required, as carbonaceous material can constitute up to 90% of the total aerosol, 10-70% of which is water soluble. Therefore it is necessary to characterize the water soluble organic carbon fraction by CCN activation, droplet growth kinetics, and surface tension measurements. In this thesis, we investigate the water soluble properties, such as surface tension, solubility, and molecular weight, of laboratory and ambient aerosols and their effect on CCN formation. A mechanism called Curvature Enhanced Solubility is proposed and shown to explain the apparent increased solubility of organics. A new method, called Köhler Theory Analysis, which is completely new, fast, and uses minimal amount of sample was developed to infer the molar volume (or molar mass) of organics. Due to the success of the technique in predicting the molar volume of laboratory samples, it was applied to aerosols collected in Mexico City. Additionally the surface tension, CCN activity, and droplet growth kinetics of these urban polluted aerosols were investigated. Studies performed for the water soluble components showed that the aerosols in Mexico City have surfactants present, can readily become CCN, and have growth similar to ammonium sulfate. Finally, aerosols from three different polluted sources, urban, bovine, and ship emissions, were collected and characterized. The data assembled was used to predict CCN concentrations and access our understanding of the system. From these analyses, it was evident that knowledge of the chemical composition and mixing state of the aerosol is necessary to achieve agreement between observations and predictions. The data obtained in this thesis can be introduced and used as constraints in aerosol-cloud interaction parameterizations developed for global climate models, which could lead to improvements in the indirect effect of aerosols.