4.6 Article

Desalination-of water by vapor-phase transport through hydrophobic nanopores

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JOURNAL OF APPLIED PHYSICS
卷 108, 期 4, 页码 -

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AMER INST PHYSICS
DOI: 10.1063/1.3419751

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  1. King Fahd University of Petroleum and Minerals in Dhahran, Saudi Arabia through the Center for Clean Water and Clean Energy at MIT and KFUPM

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We propose a new approach to desalination of water whereby a pressure difference across a vapor-trapping nanopore induces selective transport of water by isothermal evaporation and condensation across the pore. Transport of water through a nanopore with saline water on one side and pure water on the other side under a pressure difference was theoretically analyzed under the rarefied gas assumption using a probabilistic framework that accounts for diffuse scattering from the pore walls as well as reflection from the menisci. The analysis revealed that in addition to salinity, temperature, and pressure difference, the nanopore aspect ratio and the probability of condensation of a water molecule incident on a meniscus from the vapor phase, known as the condensation coefficient, are key determinants of flux. The effect of condensation coefficient on mass flux becomes critical when the aspect ratio is small. However, the mass flux becomes independent of the condensation coefficient as the pore aspect ratio increases, converging to the Knudsen flux for long nanopores. For design of a nanopore membrane that can trap vapor, a minimum aspect ratio is derived for which coalescence of the two interfaces on either side of the nanopore remains energetically unfavorable. Based on this design criterion, the analysis suggests that mass flux in the range of 20-70 g/m(2) s may be feasible if the system is operated at temperatures in the range of 30-50 degrees C. The proposed approach further decouples transport properties from material properties of the membrane, which opens the possibility of engineering membranes with appropriate materials that may lead to reverse osmosis membranes with improved flux, better selectivity, and high chlorine resistance. (C) 2010 American Institute of Physics. [doi:10.1063/1.3419751]

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