Application Of Polymeric Membranes Research Articles

Coated wire ion-selective electrode for palladium(II) and its application to catalyst analysis

The construction, performance and application of polymeric membrane (PME) and coated wire (CWE) palladium(II)-selective electrodes based on the ion pair between tetra bromopalladate(II) and hexadecylpyridinium cation (HDP +) in a poly(vinyl chloride) matrix, plasticized with o-NPOE are described. The influence of membrane composition, bromide ion concentration and pH on the potentiometric responses of electrodes were investigated. Nernstian responses were obtained for the two type of electrodes with low limits of detection (1.0×10 −6 M for PME and 5.0×10 −8 M for CWE). The potentiometric responses are independent of the pH of test solution in the range 3–8. The response time of electrodes are fast (30 s for PME and 10 s for CWE), and they can be used for at least 3 months without any considerable divergence in potentials. The proposed electrodes revealed good selectivity for palladium(II) respect to different cations and anions. They were used to the direct potentiometric determination of palladium(II) in silicon-alumina catalysts.

Nanofilter for hydrogen purification

The application of polymeric membranes in combination with metallic films can be used for gas purification, in particular hydrogen (Int J Hydrogen Energy 27(2) (2002) 905), whose molecules are very small. The affinity of hydrogen to certain metals supports its flow, but restricts the permeation of other gases. However, the flow rate is very small in dense membranes. Attempts have been made to etch nuclear tracks created in polymeric foils, from both sides in a very controlled way such that conical etched pits meet at their vertices. This has been characterized by gas permeation measurements. The low density of 10 6 – 10 8 tracks/ cm 2 is generated by a 60 MeV carbon ion beam at the NSC Pelletron, New Delhi. The primary ion fluence of 10 10/ cm 2 was reduced by means of a gold absorber foil. The gas flow rate has shown a considerable improvement along with the selectivity of hydrogen over the carbon dioxide where the molecular sizes of 0.21 and 0.4 nm , respectively, are separable.

Structure–property relationships for liquid transport in modified polypropylene membranes

AbstractIn view of the intensifying interest in the application of polymeric membranes in mixture separation processes, the permeation and permselective properties of polypropylene films toward several candidate organic liquids and vapors were investigated. Polymer films were subjected to solvent and thermal treatments, and the effects of these treatments on film morphology and transport properties were studied. Structure–property relationships for membrane permeation were then developed. Polypropylene films were found to be selective toward toluene, relative to isooctane, and p‐xylene relative to o‐xylene. Liquid flux rates were found to depend primarily upon the solubility of the permeants in the films and the absolute difference in the solubility parameters of the polymer–liquid pair provided a good basis for correlation of this effect. Considering liquids of closely similar solubility parameters, fluxes were found to be dependent upon the apparent molecular cross sections of the permeants. Films annealed in various organic solvents at temperatures of 60–100°C exhibited enhanced permeability, with up to fifteenfold increase relative to untreated membranes, but with reduced selectivity towards the permeants. A mechanism to account for these effects through consideration of the influence of treating solvent type on polymer morphology is proposed. It postulates the formation of more open or coarser spherulitic structures as a result of recrystallization in the presence of solvent during annealing. The enhanced flux rates in the treated films are attributed to the changes in the spherulite textures and to diminished intercrystalline tie chain constrainment within the spherulitic substructure.