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Gas permeation properties for organosilica membranes with different Si/C ratios and evaluation of microporous structures
Authors:Masakoto Kanezashi  Yuri Yoneda  Hiroki Nagasawa  Toshinori Tsuru  Kazuki Yamamoto  Joji Ohshita
Affiliation:1. Dept. of Chemical Engineering, Graduate School of Engineering, Hiroshima University, Higashi‐Hiroshima, Japan;2. Dept. of Applied Chemistry, Graduate School of Engineering, Hiroshima University, Higashi‐Hiroshima, Japan
Abstract:Organosilica membranes were fabricated using bridged organoalkoxysilanes (bis(triethoxysilyl)methane (BTESM), bis(triethoxysilyl)ethane (BTESE), bis(triethoxysilyl)propane (BTESP), bis(trimethoxysilyl)hexane (BTMSH), bis(triethoxysilyl)benzene (BTESB), and bis(triethoxysilyl)octane (BTESO)) to produce highly permeable molecular sieving membranes. The effect of the organoalkoxysilanes on network pore size and microporous structure was evaluated by examining the molecular size and temperature dependence of gas permeance across a wide range of temperatures. Organosilica membranes showed H2/N2 and H2/CH4 permeance ratios that ranged from 10 to 150, corresponding to network pore size, and both H2 selectivity decreased with an increase in the carbon number between 2 Si atoms. Organosilica membranes showed activated diffusion for He and H2, and a slope of temperature dependence that increased approximate to the increase in the carbon number between 2 Si atoms. The relationship between activation energy and He/H2 permeance ratio for SiO2 and organosilica membranes suggested that the molecular sieving can dominate He and H2 permeation properties via the rigid microporous structure, which was constructed by BTESM and BTESE. With increased in the carbon concentration in silica, polymer chain vibration in organic bridges, which is a kind of solution/diffusion mechanism, can dominate the permeation properties. © 2017 American Institute of Chemical Engineers AIChE J, 63: 4491–4498, 2017
Keywords:sol‐gel method  organosilica membrane  pore‐size control  gas permeation  activation energy
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