Thin-film membranes derived from co-continuous polymer blends: preparation and performance

Abstract

Two approaches for preparing thin-film membranes from immiscible co-continuous polymer blends are presented. Approach 1 involves the melt blending of co-continuous polymer blends followed by the selective extraction of one of the phases and results in a microporous membrane material of high void volume. In that case, the pore size is defined by the phase size of one of the phases in the blend and hence composition, interfacial tension, viscosity ratio and other parameters influencing phase morphology can be used to control porosity. For that first approach, the blend system studied is high density polyethylene/polystyrene, compatibilized with SEBS (styrene–ethylene–buthylene–styrene) triblock copolymer. Both symmetric and asymmetric type membranes can be obtained. The symmetric membrane demonstrates porosity ranging from 80 to 230 nm. It is shown that extraction time can be used to develop asymmetry in the membrane and the effects of extraction time on the morphology, pore size distribution and performance are presented. High flux values and high apparent rejection factors estimated from permeability testing indicate that these materials could have potential in a variety of membrane applications.Approach 2 is a solventless approach that results in a membrane of very low void volume. A high interfacial tension immiscible co-continuous blend compatibilized at different levels by a weak interfacial modifier is prepared by melt mixing and extrusion through a sheet die. Microporosity in the bulk of the material is generated in situ during cooling by this approach. The thin sheet is then subjected to uniaxial or biaxial cold stretching to develop surface porosity. This technique exploits interfacial debonding and the weak interface of the co-continuous morphology acts as a template to guide the direction of porosity development. Highly percolated membranes of polycarbonate and high-density polyethylene with SEBS were prepared. These membranes possess pore sizes in the range of 100 nm and are of very low void volume. Oxygen permeation tests, carried out under atmospheric pressure, demonstrate a dramatic increase in oxygen flux from 1378 cm3/m2/day (non-stretched 50PE/50PC/15SEBS sample) to 106,270 cm3/m2/day (biaxially stretched sample). The results indicate that they could have potential as breathable barrier type materials. The effects of draw ratio on the permeation values are presented.