Showing papers on "Permeation published in 2018"

Functionalized boron nitride membranes with ultrafast solvent transport performance for molecular separation

Abstract: Pressure-driven, superfast organic solvent filtration membranes have significant practical applications. An excellent filtration membrane should exhibit high selectivity and permeation in aqueous and organic solvents to meet increasing industrial demand. Here, we report an amino functionalized boron nitride (FBN) based filtration membrane with a nanochannel network for molecular separation and permeation. This membrane is highly stable in water and in several organic solvents and shows high transport performance for solvents depending on the membranes' thickness. In addition, the FBN membrane is applicable for solute screening in water as well as in organic solvents. More importantly, the FBN membranes are very stable in acidic, alkaline and oxidative media for up to one month. The fast-flow rate and good separation performance of the FBN membranes can be attributed to their stable networks of nanochannels and thin laminar structure, which provide the membranes with beneficial properties for practical separation and purification processes.

Electrically controlled water permeation through graphene oxide membranes.

Abstract: Developing 'smart' membranes that allow precise and reversible control of molecular permeation using external stimuli would be of intense interest for many areas of science: from physics and chemistry to life-sciences. In particular, electrical control of water permeation through membranes is a long-sought objective and is of crucial importance for healthcare and related areas. Currently, such adjustable membranes are limited to the modulation of wetting of the membranes and controlled ion transport, but not the controlled mass flow of water. Despite intensive theoretical work yielding conflicting results, the experimental realisation of electrically controlled water permeation has not yet been achieved. Here we report electrically controlled water permeation through micrometre-thick graphene oxide (GO) membranes. By controllable electric breakdown, conductive filaments are created in the GO membrane. The electric field concentrated around such current carrying filaments leads to controllable ionisation of water molecules in graphene capillaries, allowing precise control of water permeation: from ultrafast permeation to complete blocking. Our work opens up an avenue for developing smart membrane technologies and can revolutionize the field of artificial biological systems, tissue engineering and filtration.

Electrically controlled water permeation through graphene oxide membranes

Abstract: Controlled transport of water molecules through membranes and capillaries is important in areas as diverse as water purification and healthcare technologies1–7. Previous attempts to control water permeation through membranes (mainly polymeric ones) have concentrated on modulating the structure of the membrane and the physicochemical properties of its surface by varying the pH, temperature or ionic strength3,8. Electrical control over water transport is an attractive alternative; however, theory and simulations9–14 have often yielded conflicting results, from freezing of water molecules to melting of ice14–16 under an applied electric field. Here we report electrically controlled water permeation through micrometre-thick graphene oxide membranes17–21. Such membranes have previously been shown to exhibit ultrafast permeation of water17,22 and molecular sieving properties18,21, with the potential for industrial-scale production. To achieve electrical control over water permeation, we create conductive filaments in the graphene oxide membranes via controllable electrical breakdown. The electric field that concentrates around these current-carrying filaments ionizes water molecules inside graphene capillaries within the graphene oxide membranes, which impedes water transport. We thus demonstrate precise control of water permeation, from ultrafast permeation to complete blocking. Our work opens up an avenue for developing smart membrane technologies for artificial biological systems, tissue engineering and filtration.

Franz Diffusion Cell Approach for Pre-Formulation Characterisation of Ketoprofen Semi-Solid Dosage Forms.

Abstract: This study aimed to evaluate and compare, using the methodology of Franz diffusion cells, the ketoprofen (KTP) releasing profiles of two formulations: A gel and a conventional suspension. The second aim was to show that this methodology might be easily applied for the development of semi-solid prototypes and claim proof in pre-formulation stages. Drug release analysis was carried out under physiological conditions (pH: 5.6 to 7.4; ionic strength 0.15 M; at 37 °C) for 24 h. Three independent vertical Franz cells were used with a nominal volume of the acceptor compartment of 125 mL and a diffusion area of 2.5 cm2. Additionally, two different membranes were evaluated: A generic type (regenerated cellulose) and a transdermal simulation type (Strat-M®). The KTP permeation profiles demonstrated that depending on the membrane type and the vehicle used, the permeation is strongly affected. High permeation efficiencies were obtained for the gel formulation, and the opposite effect was observed for the suspension formulation. Moreover, the permeation studies using Strat-M membranes represent a reproducible methodology, which is easy to implement for pre-formulation stage or performance evaluation of semi-solid pharmaceutical products for topical or transdermal administration.

Enhanced CO2/CH4 Separation Performance of a Mixed Matrix Membrane Based on Tailored MOF-Polymer Formulations

Abstract: Membrane-based separations offer great potential for more sustainable and economical natural gas upgrading. Systematic studies of CO2/CH4 separation over a wide range of temperatures from 65 °C (338 K) to as low as -40 °C (233 K) reveals a favorable separation mechanism toward CO2 by incorporating Y-fum-fcu-MOF as a filler in a 6FDA-DAM polyimide membrane. Notably, the decrease of the temperature from 308 K down to 233 K affords an extremely high CO2/CH4 selectivity (≈130) for the hybrid Y-fum-fcu-MOF/6FDA-DAM membrane, about four-fold enhancement, with an associated CO2 permeability above 1000 barrers. At subambient temperatures, the pronounced CO2/CH4 diffusion selectivity dominates the high permeation selectivity, and the enhanced CO2 solubility promotes high CO2 permeability. The differences in adsorption enthalpy and activation enthalpy for diffusion between CO2 and CH4 produce the observed favorable CO2 permeation versus CH4. Insights into opportunities for using mixed-matrix membrane-based natural gas separations at extreme conditions are provided.

Functionally graded membranes from nanoporous covalent organic frameworks for highly selective water permeation

Abstract: Natural materials are often arranged in intricate gradient architectures to implement specific functionalities. Implanting such an exquisite prototype into synthetic membranes remains a grand challenge in real-world applications. In this study, functionally graded membranes are fabricated through a surface segregation method using 2D nanoporous COF TpHZ and poly(ether sulfone) as composite building blocks. During the membrane formation, the COF nanosheets can spontaneously migrate from the membrane bulk to the membrane surface to form a gradient distribution, which can be varied by manipulating the COF addition content and phase inversion temperature. The highest COF content on the membrane surface can be up to 50.90 vol%. Due to the formation of a graded structure, the membranes are endowed with remarkably increased hydrophilicity and free volume characteristics. Accordingly, the optimized membrane exhibits a permeation flux of 2.48 kg m−2 h−1 and a high separation factor of 1430, and remains robust during a stability test for 320 h, and is one of the most efficient mixed matrix membranes for water/ethanol separation. The separation factor is two orders of magnitude more than that of existing commercial membranes. The concept of functionally graded membranes can be applicable to the development of a broad range of high-performance materials.

The synthesis, chain-packing simulation and long-term gas permeability of highly selective spirobifluorene-based polymers of intrinsic microporosity

Abstract: Membranes composed of Polymers of Intrinsic Microporosity (SBF-PIMs) have potential for commercial gas separation. Here we report a combined simulation and experimental study to investigate the effect on polymer microporosity and gas permeability by placing simple substituents such as methyl, t-butyl and fused benzo groups onto PIMs derived from spirobifluorene (PIM-SBFs). It is shown that methyl or t-butyl substituents both cause a large increase in gas permeabilities with four methyl groups enhancing the concentration of ultramicropores ( 1.0 nm). Long-term ageing studies (>3.5 years) demonstrate the potential of PIM-SBFs as high-performance membrane materials for gas separations. In particular, the data for the PIM derived from tetramethyl substituted SBF reaches the proposed 2015 Robeson upper bound for O2/N2 and, hence, hold promise for the oxygen or nitrogen enrichment of air. Mixed gas permeation measurements for CO2/CH4 of the aged PIM-SBFs also demonstrate their potential for natural gas or biogas upgrading.

Removal of metal ions and humic acids through polyetherimide membrane with grafted bentonite clay

Abstract: Functional surfaces and polymers with branched structures have a major impact on physicochemical properties and performance of membrane materials. With the aim of greener approach for enhancement of permeation, fouling resistance and detrimental heavy metal ion rejection capacity of polyetherimide membrane, novel grafting of poly (4-styrenesulfonate) brushes on low cost, natural bentonite was carried out via distillation-precipitation polymerisation method and employed as a performance modifier. It has been demonstrated that, modified bentonite clay exhibited significant improvement in the hydrophilicity, porosity, and water uptake capacity with 3 wt. % of additive dosage. SEM and AFM analysis showed the increase in macrovoides and surface roughness with increased additive concentration. Moreover, the inclusion of modified bentonite displayed an increase in permeation rate and high anti-irreversible fouling properties with reversible fouling ratio of 75.6%. The humic acid rejection study revealed that, PEM-3 membrane having rejection efficiency up to 87.6% and foulants can be easily removed by simple hydraulic cleaning. Further, nanocomposite membranes can be significantly employed for the removal of hazardous heavy metal ions with a rejection rate of 80% and its tentative mechanism was discussed. Conspicuously, bentonite clay-bearing poly (4-styrenesulfonate) brushes are having a synergistic effect on physicochemical properties of nanocomposite membrane to enhance the performance in real field applications.

A highly rigid and gas selective methanopentacene-based polymer of intrinsic microporosity derived from Tröger's base polymerization

Abstract: Polymers of intrinsic microporosity (PIMs) have been identified as potential next generation membrane materials for the separation of gas mixtures of industrial and environmental relevance. Based on the exceptionally rigid methanopentacene (MP) structural unit, a Polymer of Intrinsic Microporosity (PIM-MP-TB) was designed to demonstrate high selectivity for gas separations. PIM-MP-TB was prepared using a polymerisation reaction involving the formation of Troger's base linking groups and demonstrated an apparent BET surface area of 743 m2 g−1 as a powder. The microporosity of PIM-MP-TB was also characterized by chain packing simulations. PIM-MP-TB proved soluble in chlorinated solvents and was cast as a robust, free-standing film suitable for gas permeation measurements. Despite lower gas permeability as compared to previously reported PIMs, high selectivities for industrially relevant gas pairs were obtained, surpassing the 2008 Robeson upper bound for H2/CH4 and O2/N2, (e.g., PO2 = 999 Barrer; αO2/N2 = 5.0) and demonstrating a clear link between polymer rigidity and selectivity. Upon aging, the permeability data move parallel to the Robeson upper bounds with a decrease of permeability, compensated by a related increase in selectivity. Mixed gas permeation measurement for CO2/CH4 and CO2/N2 mixtures confirmed the excellent selectivity of PIM-MP-TB for potentially relevant separations such as biogas upgrading and CO2 capture from flue gas. Importantly, unlike other high performing PIMs, PIM-MP-TB is prepared in four simple steps from a cheap starting material.

Asymmetric Aerogel Membranes with Ultrafast Water Permeation for the Separation of Oil-in-Water Emulsion

Abstract: Owing to highly porous and low density attributes, aerogels have been actively utilized in catalysis and adsorption processes, but their great potential in filtration requires exploitation. In this study, an asymmetric aerogel membrane is fabricated via one-pot hydrothermal reaction-induced self-cross-linking of poly(vinyl alcohol) (PVA), which exhibits ultrafast permeation for the separation of oil-in-water emulsion. Meanwhile, carbon nanotubes are added to improve the mechanical strength of the aerogel membranes. The self-cross-linking of PVA forms the supporting layer, and the exchange of water and vapor at the interface of PVA solution and air generates the separating layer as well as abundant hydroxyl groups on the membrane surface. The density, porosity, pore size, and wettability of the aerogel membrane can be tuned by the PVA concentration. Owing to high porosity (>95%) and suitable pore size (<85 nm), the aerogel membrane exhibits high rejection (99.0%) for surfactant-stabilized oil-in-water emulsion with an ultrahigh permeation flux of 135.5 × 103 L m-2 h-1 bar-1 under gravity-driven flow, which is 2 orders of magnitude higher than commercial filtration membranes with similar rejection. Meanwhile, the aerogel membrane exhibits superhydrophilicity, superoleophobicity underwater, and excellent antifouling properties for various surfactant-stabilized oil-in-water emulsions, as indicated by the fact that the flux recovery ratio maintains more than 93% after five cycles of the filtration experiment. The findings in this study may offer a novel idea to fabricate high-throughput filtration membranes.

Effect of Film Thickness and Physical Aging on “Intrinsic” Gas Permeation Properties of Microporous Ethanoanthracene-Based Polyimides

Abstract: Two ethanoanthracene-based dianhydrides, 9,10-dimethylethanoanthracene-2,3,6,7-tetracarboxylic anhydride (EA-DA) and its more flexible dibenzodioxane-containing derivative (EAD-DA), were synthesized from the same starting material, 9,10-dimethyl-ethanoanthracene-2,3,6,7-tetraol, and used for the preparation of bicyclic intrinsically microporous polyimides (PIM-PIs) by one-pot polycondensation reaction with 3,3′-dimethylnaphthidine (DMN). The resulting organosoluble polyimides, EA-DMN and EAD-DMN, were thermally stable up to 300 °C and had good mechanical properties with tensile strength of 55 and 63 MPa and elongation at break of 15 and 30%, respectively. EA-DMN and EAD-DMN polyimides displayed Brunauer–Emmett–Teller (BET) surface areas of 720 and 800 m2 g–1, respectively. Fresh films showed promising gas separation performance with very high gas permeabilities and moderate gas-pair selectivities, which were both strongly dependent on film thickness. The results obtained in this study shed more light on t...