4.2 Article Proceedings Paper

Diffusion Control of Porous Membrane by Modifying the Nanopore Properties

Journal

JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY
Volume 11, Issue 2, Pages 1656-1659

Publisher

AMER SCIENTIFIC PUBLISHERS
DOI: 10.1166/jnn.2011.3303

Keywords

Nanoporous Materials; Surface Modification; Nanopore; Diffusion

Funding

  1. National Research Foundation of Korea [R31-2011-000-10010-0, 2008-0057903, 핵06A3006] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  2. Rural Development Administration (RDA), Republic of Korea [PJ00692120111142300] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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We have investigated the diffusion of various solvents on nanoporous membranes with various pore size and surface energy. We have modified the size of pore channel and surface energy of porous membrane through grafting different sized alkyl chain on inorganic membranes. Typically, disc type zirconia membranes with pore size of 3 nm and silica ones with 1 nm pore were purchased from Inocermic Co. Ltd. (Germany), and the surface and pore channel was modified by either octyltriethoxysilane (OTS) with chain length similar to 1 nm or pentyltriethoxysilane (PTS) with chain length similar to 0.5 nm. The water contact angles of both OTS and PTS grafted membrane were larger than 100 degrees indicating the hydrophobically modified surface. Contact angles of hydrophilic and hydrophobic solvents were also examined to obtain exact surface energy (gamma(SV)) of grafted membrane, and the values were determined to be 56.3, 45.3, and 42.2 mN/m for ungrafted, PTS- and OTS-grafted membrane, respectively. The solvent diffusion patterns were evaluated by measuring the concentration gradient of small dye molecule, azobenzene. The diffusion coefficients of various solvents were measured on the basis of Fick's diffusion law. It was concluded that the diffusivity is dependent on the pore size for solvent with low surface tension and on the gamma(SV) value for solvent with high surface tension.

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