Abstract
Polyamide thin-film composite membranes were prepared on a reinforced microporous polyethersulfone (PES) support by in situ interfacial polycondensation of amic acid diamines (AADs) with 1,3,5-benzenetricarbonyl trichloride and subsequent curing. Water soluble AADs were synthesized by reacting trimellitic anhydride chloride and cyclic/aromatic diamines in dimethylformamide at 5–10°C. Polyamide ultra-thin barrier layer containing different structural modifications were isolated by dissolving the matrix PES support in dichloromethane and characterized for IR, NMR, and DSC techniques. Morphology of membranes by scanning electron microscopy showed the appearance of honeycomb-like structure on the polyamide skin surface and the cross section displayed the presence of nodular structure which arises from the dense polyamide skin. The performances of these membranes were measured by passing the feed solutions containing 2,000 ppm of NaCl and Na2SO4 in a reverse osmosis test kit. Membranes exhibited very broad range of separations for NaCl (35–85%) and Na2SO4 (40–89%) depending on the chemical nature of the AADs. The glass transition temperature (Tg) of composite membranes with aromatic diamine structures were >220°C, indicating the higher stiffness nature of the polymer chain due to the presence of fully aromatic structural units.
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