Impact of industrial air pollution on the quality of atmospheric water production.

The atmospheric water generator (AWG) is a commercially available device that produces water from the air in large volumes over short times. This method can be applied in most regions of the world to solve chronic and acute drinking water scarcity. However, knowledge of the effects of air chemical composition on AWG-produced water quality is still very limited. In this study, a comprehensive survey of AWG-produced water quality was conducted in a heavily polluted industrial environment; 83 AWG water samples were analyzed for 99 different quality parameters, including organic, inorganic, and microbial contamination. Two parameters-nickel (15 samples) and dichloromethane (2 samples)-exceeded sporadically their drinking water standards of EPA, EU and IL. Ammonia was the only parameter consistently above standard limits of 0.5 mg/L (61% of samples, relevant to 47 countries) and even higher than 1.5 mg/L. Comparison to real air concentrations of volatile pollutants in the same environment did not reveal any significant correlations; while some pollutants were found at high concentrations in the air, this was not reflected by their presence in the produced water. The findings show that even in areas that are considered excessively polluted relative to the natural environment, the water produced from the air by AWG could be considered suitable for drinking, with careful attention to very specific contaminants.

Aqueous stability of alumina and silica perhydrate hydrogels: experiments and computations.

Alumina and silica perhydrate hydrogels were synthesized. Raman spectroscopy and solid (27)Al MAS NMR confirmed alumina perhydrate formation. Thermal and aqueous stability of alumina and silica perhydrates was studied, and they showed exceptionally high stabilities. Alumina perhydrate retained some of the hydrogen peroxide even at 170 °C, higher than any other reported perhydrate, whereas the silica perhydrate lost its hydrogen peroxide content already at 90 °C. The silica perhydrate lost all its peroxide content upon immersion in water, whereas the alumina perhydrate was stable under near-neutral pH conditions. A computational study was conducted in order to glean molecular insight into the observed thermal and aqueous stability of alumina compared to silica perhydrate. Comparison of the hydrogen bond features and the stabilization energies of the hydrate and perhydrate of silica and alumina revealed a higher preference for hydrogen peroxide over water by alumina relative to silica. This is shown to be due to hydrogen peroxide being a better hydrogen donor than water and due to the superior hydrogen accepting propensity of alumina compared to silica.

Zinc dioxide nanoparticulates: a hydrogen peroxide source at moderate pH.

Solid peroxides are a convenient source of hydrogen peroxide, which once released can be readily converted to active oxygen species or to dissolved dioxygen. A zinc peroxide nanodispersion was synthesized and characterized, and its solubility was determined as a function of pH and temperature. We show that zinc peroxide is much more stable in aqueous solutions compared to calcium and magnesium peroxides and that it retains its peroxide content down to pH 6. At low pH conditions H2O2 release is thermodynamically controlled and its dissolution product, Zn(2+), is highly soluble, and thus, hydrogen peroxide release can be highly predictable. The Gibbs free energy of formation of zinc peroxide was found to be -242.0 ± 0.4 kJ/mol and the enthalpy of formation was -292.1 ± 0.7 kJ/mol, substantially higher than theoretically predicted before. The biocidal activity of zinc peroxide was determined by inactivation studies with Escherichia coli cultures, and the activity trend agrees well with the thermodynamic predictions.