Permeation of CO2 and N2 through glassy poly(dimethyl phenylene) oxide under steady- and presteady-state conditions

Glassy polymers are often used for gas separations because of their high selectivity. Although the dual-mode permeation model correctly fits their sorption and permeation isotherms, its physical interpretation is disputed, and it does not describe permeation far from steady state, a condition expected when separations involve intermittent renewable energy sources. To develop a more comprehensive permeation model, we combine experiment, molecular dynamics, and multiscale reaction–diffusion modeling to characterize the time-dependent permeation of N2 and CO2 through a glassy poly(dimethyl phenylene oxide) membrane, a model system. Simulations of experimental time-dependent permeation data for both gases in the presteady-state and steady-state regimes show that both single- and dual-mode reaction–diffusion models reproduce the experimental observations, and that sorbed gas concentrations lag the external pressure rise. The results point to environment-sensitive diffusion coefficients as a vital characteristic of transport in glassy polymers

Permeation of CO₂ and N₂ through glassy poly(dimethyl phenylene) oxide under steady- and presteady-state conditions

Glassy polymers are often used for gas separations because of their high selectivity. Although the dual‐mode permeation model correctly fits their sorption and permeation isotherms, its physical interpretation is disputed, and it does not describe permeation far from steady state, a condition expected when separations involve intermittent renewable energy sources. To develop a more comprehensive permeation model, we combine experiment, molecular dynamics, and multiscale reaction–diffusion modeling to characterize the time‐dependent permeation of N₂ and CO₂ through a glassy poly(dimethyl phenylene oxide) membrane, a model system. Simulations of experimental time‐dependent permeation data for both gases in the presteady‐state and steady‐state regimes show that both single‐ and dual‐mode reaction–diffusion models reproduce the experimental observations, and that sorbed gas concentrations lag the external pressure rise. The results point to environment‐sensitive diffusion coefficients as a vital characteristic of transport in glassy polymers

Gas separation properties of a thermally stable and chemically resistant polytriazole membrane

The polymer poly (1,3-phenyl-1,4-phenyl)-4-phenyl-1,3,4-triazole has been investigated for its gas separation properties. This thermally stable and chemically resistant polymer can be processed into membranes by the phase-inversion technique because of its unexpectedly good solubility in formic acid. Homogeneous membranes have been tested with respect to their permeability for several gases, and the influence of time and temperature upon permeation has been investigated. The polymer shows reasonable permeabilities for several gases and excellent selectivities. After a conditioning time of several days in which the permeability of the faster-moving gases increases by a factor of about 2, the permeation properties of the polymer remain constant for at least two months. A thermal treatment at 295°C, just above the glass transition temperature, can reduce the conditioning time and can prevent the film from shrinkage at high permeation temperatures without affecting the permeation properties

Glycerol Modulates Water Permeation through Escherichia coli Aquaglyceroporin GlpF

Among aquaglyceroporins that transport both water and glycerol across the cell membrane, Escherichia coli glycerol uptake facilitator (GlpF) is the most thoroughly studied. However, one question remains: Does glycerol modulate water permeation? This study answers this fundamental question by determining the chemical-potential profile of glycerol along the permeation path through GlpF's conducting pore. There is a deep well near the Asn-Pro-Ala (NPA) motifs (dissociation constant 14 microM) and a barrier near the selectivity filter (10.1 kcal/mol above the well bottom). This profile owes its existence to GlpF's perfect steric arrangement: The glycerol-protein van der Waals interactions are attractive near the NPA but repulsive elsewhere in the conducting pore. In light of the single-file nature of waters and glycerols lining up in GlpF's amphipathic pore, it leads to the following conclusion: Glycerol modulates water permeation in the microM range. At mM concentrations, GlpF is glycerol-saturated and a glycerol dwelling in the well occludes the conducting pore. Therefore, water permeation is fully correlated to glycerol dissociation that has an Arrhenius activation barrier of 6.5 kcal/mol. Validation of this theory is based on the existent in vitro data, some of which have not been given the proper attention they deserved: The Arrhenius activation barriers were found to be 7 kcal/mol for water permeation and 9.6 kcal/mol for glycerol permeation; The presence of up to 100 mM glycerol did not affect the kinetics of water transport with very low permeability, in apparent contradiction with the existent theories that predicted high permeability (0 M glycerol)

High performance blended membranes using a novel preparation technique

The possibility of applying novel microwave (MW) technique in the dissolution of polyethersulfone (PES) and lithium halides in aprotic solvent is studied. The lithium halides additives used are lithium fluoride (LiF), lithium bromide (LiBr) and lithium chloride (LiCl) and a comparison is made with conventional method. PES was dissolved in dimethylformamide (DMF) in the single solvent whilst for the double solvent (DS); PES was dissolved in a mixture of two different solvents DMF and acetone. The concentrations of lithium halide in both solvents were varied from 1 to 5 wt%. In order to illuminate the mechanism through which lithium halide influences the kinetic membrane performance in both techniques, rheological, FTIR, contact angle and water uptake analysis were performed. The performances of the membranes were evaluated in terms of pure water permeation (PWP), permeation rate (PR) and separation rates of various polyethylene glycols. Result revealed that the hollow fiber MW membrane with the 3 wt% LiBr additive exhibits both high permeation rates of 222.16 Lm-2hr-1 and separation rates of 99% and molecular weight cutoff (MWCO) of 2.6 kDa. In general, the MW membranes exhibited higher permeation and separation rates compared to conventional electrothermal heating (CEH) membranes. The FTIR, contact angle and water uptake measurement revealed that the LiCl and LiBr have enhanced the hydrophilic properties of the PES membranes thus producing membrane with high permeation and separation rates

Strategies for studying permeation at voltage-gated ion channels

Voltage-dependent ion channels are presently thought to consist of several distinct functional regions: (a) activation gates, (b) inactivation gates, and permeation pathways. This chapter focuses on permeation pathways and may spur new ideas about experiments that use site-directed mutagenesis to probe the ion conduction pathway. Some hubris is required to attempt a survey of this field since individual families -- K^+, Na^+, or Ca^(2+) -- have been reviewed in detail (15, 68, 115, 127). My unified treatment is motivated by the structural similarity suggested by recent cDNA sequencing data on this group (see, for instance, 24). There have been many excellent previous treatments of ion channel permeation (6, 15, 34, 35, 51, 53, 68, 73, 74, 115, 127)

Permeation through a lamellar stack of lipid mixtures

We study material transport and permeation through a lamellar stack of multi-component lipid membranes by performing Monte Carlo simulations of a stacked two-dimensional Ising model in presence of permeants. In the model, permeants are transported through the stack via in-plane lipid clusters, which are inter-connected in the vertical direction. These clusters are formed transiently by concentration fluctuations of the lipid mixture, and the permeation process is affected, especially close to the critical temperature of the binary mixture. We show that the permeation rate decays exponentially as function of temperature and permeant lateral size, whereas the dependency on the characteristic waiting time obeys a stretched exponential function. The material transport through such lipid clusters can be significantly affected around physiological temperatures.Comment: Accepted versio

Financial permeation as a role of microfinance : has microfinance actually been helpful to the poor?

This article is distinct in its application of the logit transformation to the poverty ratio for the purpose of empirically examining whether the financial sector helps improve standards of living for low-income people. We propose the term financial permeation to describe how financial networks expand to spread money among the poor. We measure financial permeation by three indicators related to microfinance institutions (MFIs) and then examine its effect on poverty reduction at the macro level using panel data for 90 developing countries from 1995 to 2008. We find that financial permeation has a statistically significant and robust effect on decreasing the poverty ratio.Developing countries, Microfinance, Poverty, Poverty reduction, Financial permeation, Microfinance, Panel Data