Modification of cellulose acetate reverse osmosis membranes by radiation grafting

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Abstract
Large excesses of a chain transfer agent, carbon tetrachloride, were introduced to a recipe for the mutual radiation grafting of styrene to cellulose acetate film. The effect of the carbon tetrachloride on the molecular characteristics as well as the reverse osmosis and time dependent mechanical properties of resulting graft copolymers was determined. Extremely short side chains were generated as a consequence of the high concentrations of chain transfer agent and the composite results further suggest that the morphology of the grafted films is best described as “destructured” or internally plasticized consequent to grafting in the presence of CCl4. Reverse osmosis fluxes increased with percent graft; salt rejection was high and unaffected by per cent graft up to 40% graft; and the tensile creep under wet conditions was significantly retarded by the grafting. These effects were shown to accrue from grafting per se by control experiments involving α‐methylstyrene which will not propagate to form a polymer under these conditions. These results are compared and contrasted with earlier work on grafting in the absence of CCl4 where long side chains of polystyrene were generated resulting in a structuring of the polymer involving domains of polystyrene‐rich material and domains of cellulose acetate rich polymer.