Membrane separation for helium extraction from natural gas gained increased interest recently. Several vendors offer membrane elements for helium extraction, although data on their performance and operating experience are unpublished. The aim of this work was to obtain and study the separation performance of asymmetric hollow-fiber membrane element from commercial polyamide-imide Torlon®, in conditions close to the industrial process of helium extraction from natural gas. A membrane element with an active area of 0.177 m2, a helium permeance of 100 l(STP)/(m2·h·bar), and a selectivity α(He/CH4) = 340 was produced. This corresponds to a selective layer thickness of 82.3 nm, which was confirmed by SEM and resistance model calculations. The obtained membrane element was employed to decrease the concentration of helium in its binary mixture with methane from 0.4% to 0.05%. A relationship of separation characteristics from transmembrane pressure is also presented. At 70 bar and a stage cut of 2.7%, the feed flow rate was 0.16 m3(STP)/h, which yielded a helium permeate concentration of 14.7%. At 80 bar, a decrease in permeance to 60 l(STP)/(m2·h·bar) and in selectivity to 240 was observed. It was shown that the main reason for aging was the increased support resistance, due to a partial compaction of pores with a radius of less than 15 nm.

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In this work, polysulfone hollow fibers with oxygen permeance 70 L (STP)/(m2·h·bar) and selectivity α(O2/N2) = 6 were obtained. A decrease in the dope solution temperature allowed to diminish macrovoids due to the increase of the dope viscosity from 15.5 Pa·s at 62 °C to 35 Pa·s at 25 °C. To reduce the fiber diameter, thereby increasing the packing density, they were spun at high linear velocities. A hollow fiber membrane element was produced with effective membrane area 2.75 m2 and packing density 53%. Its air separation performance was evaluated to bridge laboratory studies and practical application.

This work was focused on the study of hypochlorite treatment on the pore size distribution of membranes. To this end, ultrafiltration membranes from a polysulfone/polyvinylpyrrolidone blend with a sponge-like structure were fabricated and exposed to hypochlorite solutions with different active chlorine concentrations for 4 h at ambient temperature. Liquid–liquid displacement and scanning electron microscopy were employed to study the limiting and surface pores, respectively. After treatment with 50 ppm hypochlorite solution at pH = 7.2, a five-fold increase in water permeance up to 1400 L/(m2·h·bar) was observed, accompanied by a 40% increase in the limiting pore sizes and almost a three-fold increase in the porosity. After 5000 ppm treatment at pH = 11.5, a 40% rise in the maximum limiting pore size and almost a two-fold increase in the porosity and permeance was observed, whereas the mean pore size was constant. Apparently, changes in the membrane structure at pH = 11.5 were connected with polyvinylpyrrolidone (PVP) degradation and wash-out, whereas at lower pH and despite lower active chlorine concentration, this process was coupled with polysulfone (PSf) destruction and removal.