Abstract
Composite cellulose acetate (CA) membranes are widely used but their multiphase nature results in additive losses, poor mechanical strength, low chemical resistance and thermal stability, limiting their separation/purification yields. To overcome this, we fabricated monophasic hybrid membranes using a modified phase inversion technique, where tetraethylorthosilicate and 3-(aminopropyl)triethoxysilane were added to the CA casting solution. The resulting co-polymerization between CA, silanols and amine-functionalized silica groups, through sol-gel chemistry, was proved by ATR-FTIR (1118 cm−1, ν(SiOC)). The presence of propyl-amine groups increases the hydraulic permeability (3×), the rupture elongation (×1.5), and decreases the Young modulus (×1/2), due to the disruption of the CA-silica 3D network. For high propyl-amine contents this behaviour is reversed due to intensive cross-linking between CA-silica chains (decrease in 903 cm−1, ν(CH3COOC-)). The addition of silica- and amine-based structures to the CA framework increases the system degrees of freedom, opening the door to the design of new CA membranes.
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