We investigated the evolution in silver nanoparticle (AgNP) properties during a series of 10-50 day experiments on suspensions with different pH (5-9), electrolyte type (NaNO and NaCl) and concentration (2 and 6 mM), Suwannee River humic acid (SRHA) concentration (0-13.2 mg C/L), and light exposure (artificial sun light exposure for 8 h per day or dark). Of these factors, pH most influenced the AgNPs' properties as it modifies surface charge as well as AgNP dissolution and oxidation and Ag reduction reactions. As a result, particle behavior differed in basic and acidic conditions. Trends with pH varied, however, based on the electrolyte and SRHA concentration. In the presence of chloride which forms AgCl(s), for example, we observed the particle size decreased with increasing pH. The opposite was observed in identical systems in NaNO. This behavior was modified by SRHA, with increasing SRHA reducing dissolution and enhancing stability. Light exposure enhanced processes resulting in AgNP dissolution, resulting in higher dissolved Ag concentrations than under similar conditions in the dark. Overall, our results highlight how AgNP properties evolve over time and provide insight needed to confidently extend model system behavior to predict the environmental fate of AgNPs.
Developments of membrane water desalination are impeded by low water vapor flux across the membrane. We present an innovative membrane design to significantly enhance the water vapor flux. A bilayer zirconia-based membrane with a thick hierarchically-structured support and a thin functional layer is prepared using a combined freeze drying tape casting and screen printing method. The hierarchically-structured YSZ support has a porosity of 42.6%, pores of 4.5 μm or larger, and a relatively low tortuosity of 1.58 along the thickness direction. The bilayer membrane is then converted from naturally hydrophilic to hydrophobic via grafting with a fluoroalkylsilane. A water flux of 28.7 Lm-2 h-1 and a salt rejection of 99.5% are achieved by exposing the functional layer to 80 o C salt water of 2 wt.% NaCl and the support layer to 20 o C distilled water. These results are the best performing ones for ceramic membranes in direct contact membrane distillation operation.
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