Jongok Won

Zeolite-filled polyimide membrane containing 2,4,6-triaminopyrimidine

Abstract Interfacial void-free Matrimid polyimide (PI) membranes filled with zeolites were prepared by introducing 2,4,6-triaminopyrimidine (TAP). TAP enhanced the contact of zeolite particles with polyimide chains presumably by forming hydrogen bonding between them. The threshold amount of TAP, needed to depress totally the void formation, varied with zeolite type in the order of zeolite 4A≈13X

Synergistic Catalytic Effect of a Composite (CoS/PEDOT:PSS) Counter Electrode on Triiodide Reduction in Dye-Sensitized Solar Cells

Inorganic/organic nanocomposite counter electrodes comprised of sheetlike CoS nanoparticles dispersed in polystyrenesulfonate-doped poly(3,4-ethylenedioxythiophene (CoS/PEDOT:PSS) offer a synergistic effect on catalytic performance toward the reduction of triiodide for dye-sensitized solar cells (DSSCs), yielding 5.4% power conversion efficiency, which is comparable to that of the conventional platinum counter electrode (6.1%). The electrochemical impedance spectroscopy (EIS) and cyclic voltammetry measurements revealed that the composite counter electrodes exhibited better catalytic activity, fostering rate of triiodide reduction, than that of pristine PEDOT: PSS electrode. The simple preparation of composite (CoS/PEDOT:PSS) electrode at low temperature with improved electrocatalytic properties are feasible to apply in flexible substrates, which is at most urgency for developing novel counter electrodes for lightweight flexible solar cells.

Structural characterization and surface modification of sulfonated polystyrene–(ethylene–butylene)–styrene triblock proton exchange membranes

Structural characteristics and membrane performance of polystyrene-block-poly(ethylene-ran-butylene)-block-polystyrene (sSEBS) copolymer proton exchange membranes in water-swollen and different ratio of water/methanol-swollen are studied by small angle X-ray scattering (SAXS), ATR FT-IR, AFM. SAXS profile of sSEBS membrane showed that microstructure was a hexagonally cylindrical structure and it was maintained in the existence of methanol in water until 30 wt.%. As the main interest was on the development of proton exchange membranes for fuel cells operating at lower temperature with liquid methanol feed, a selective thin layer was introduced on the top of sSEBS membrane by simple plasma treatment in the presence of maleic anhydride in order to prevent methanol crossover. Both methanol permeability and proton conductivity gradually decreased with increasing loading amounts of maleic anhydride. Hydrophobic anhydride properties on the top of sSEBS membrane act as a barrier for methanol but also for proton, resulting in decreasing methanol permeability and proton conductivity. The hydrolysis of anhydride groups to carboxylic acid provides a facilitated transport site for the proton. After hydrolysis, the proton conductivity was recovered and the recovery rate of proton conductivity by hydrolysis was higher than that of methanol permeability.

Phase behavior and mechanism of membrane formation for polyimide/DMSO/water system

Abstract A macrovoid-free, sponge-like porous membrane was prepared from polyimide/DMSO/water system, whereas a finger-like membrane was obtained from a polyimide/NMP/water system by phase inversion. The sponge-like membrane structure was investigated by the thermodynamics and kinetics of the phase separation process. The rates of phase separation for both systems were similar, but their phase diagrams were significantly different. The distinct features of the phase diagram for the polyimide/DMSO/water system are: (1) extremely narrow miscibility gap, (2) close gelation point to the binodal curve, and (3) almost parallel tie-line passing through the gelation point to the polymer–solvent axis. These properties hinder the phase separation process to proceed further, i.e. the growth of the polymer-lean phase is, thus frozen or stopped in the early stages. Therefore, the membrane morphology will be determined at an earlier stage in the polyimide/DMSO/water system than polyimide/NMP/water, resulting in a macrovoid-free, sponge-like membrane.

Dye-sensitized nanocrystalline solar cells based on composite polymer electrolytes containing fumed silica nanoparticles

We report remarkably high energy conversion efficiency (4.5% at 100 mW cm(-2)) of a dye-sensitized solar cell in the solid state, using composite polymer electrolytes containing fumed silica nanoparticles.

Solution properties of poly(amic acid)–NMP containing LiCl and their effects on membrane morphologies

Abstract Physical properties of poly(amic acid) (PAA) casting solutions in N -methyl-2-pyrrolidone (NMP) containing lithium chloride (LiCl) were characterized by viscometry and dynamic light scattering (DLS) and were related to the morphological properties of asymmetric membranes prepared from these solutions. At a fixed polymer concentration, the increase in viscosity of the PAA solutions with increasing LiCl content is mainly determined by the viscosity of the salt–solvent medium, implying that the LiCl–NMP interactions are stronger than those between LiCl and PAA. Because of the strong salt–solvent interactions, complexes between LiCl and NMP are formed. The complexes reduce the solvent power of NMP for PAA inducing polymer aggregation (clustering) and/or transient cross-links in the solutions. Dynamic light scattering results for salt-containing solutions at low PAA concentrations support the existence of these aggregations. Solutions without salt showed a single relaxation, but solutions with LiCl exhibit multiple relaxation modes; two diffusional modes of cooperative and aggregates, and one angle independent transient network mode. The polymer aggregates and transient cross-links form a gel-like structure in the casting solution film and hinder macrovoid formation during phase inversion, resulting in asymmetric membranes with a primarily sponge-like structure.

Facilitated transport of ethylene across polymer membranes containing silver salt: effect of HBF4 on the photoreduction of silver ions

Abstract Silver salts dissolved in amide group containing polymer such as poly(2-ethyl-2-oxazoline) (POZ) are labile to reduce to silver metals under UV-Vis light or heat. Since the reduction of silver ions to silver nanoparticles can change the separation performance of facilitated olefin transport through polymer membranes containing silver salt, it is attempted to prohibit the reduction of silver ion. It is found that the trace of water present in silver–polymer complex membranes participates in the reduction reaction and H + ions are generated in a reversible reaction of the reduction process. In this respect, tetrafluoroboric acid (HBF 4 ) was introduced as a proton donator to suppress the reduction of silver ion. The effects of HBF 4 on the photoreduction derived by UV irradiation were characterized by mixed gas transport of ethylene/ethane, UV-Vis spectroscopy, scanning electron microscopy (SEM).

Complexation mechanism of olefin with silver ions dissolved in a polymer matrix and its effect on facilitated olefin transport.

Remarkable separation performance of olefin/paraffin mixtures was previously reported by facilitated olefin transport through silver-based polymer electrolyte membranes. The mechanism of facilitated olefin transport in solid membranes of AgCF3SO3 dissolved in poly(N-vinyl pyrrolidone) (PVP) is investigated. In silver polymer electrolyte membranes, only free anions are present up to the 2:1 mole ratio of [C=O]:[Ag], and ion pairs start to form at a ratio of 1:1, followed by higher-order ionic aggregates above a ratio of 1:2. At silver concentrations above 3:1, the propylene permeance increases almost linearly with the total silver concentration, unexpectedly, regardless of the silver ionic constituents. It was also found that all the silver constituents, including ion pairs and higher order ionic aggregates, were completely redissolved into free anions under the propylene environment; this suggests that propylene can be a good ligand for the silver cation. From these experimental findings, a new mechanism for the complexation reaction between propylenes and silver salts in silver-polymer electrolytes was proposed. The new mechanism is consistent with the linearity between the propylene permeance and the total silver concentration regardless of the kind of the silver constituents. Therefore, the facilitated propylene transport through silver-polymer electrolytes may be associated mainly with the silver cation weakly coordinated with both carbonyl oxygen atoms and propylene.

Facilitated transport of olefin through solid PAAm and PAAm-graft composite membranes with silver ions

Abstract Solid poly(acrylamide) (PAAm) composite membranes containing silver ions have been investigated for olefin/paraffin separation. The propylene permeance increased significantly for a solid PAAm/AgBF 4 composite membrane with increasing loading amount of silver ions. Silver ions in solid PAAm form reversible complexes with propylene, resulting in the facilitated transport of propylene. The propylene selectivity of 100 over propane was obtained when the mole ratio of silver ions to acrylamide unit was 1. This high separation performance would be obtained predominantly because of the high loading of the propylene carrier, silver ions. PAAm-graft/AgBF 4 composite membranes were prepared in order to improve the gas permeance. Introduction of PAAm grafts on a polysulfone microporous membrane surface was confirmed by FT-IR spectroscopy. The propylene permeance was increased through the PAAm-graft/AgBF 4 membranes compared to that through of the PAAm/AgBF 4 composite membranes, indicating the formation of ultra-thin top layer.

Surface modification of polyimide and polysulfone membranes by ion beam for gas separation

The surface carbonization of polyimide (PI) and polysulfone (PSf) by ion beam has been performed to adapt the carbon molecular sieve properties on the skin of the polymeric membranes without the deformation of the membrane structure. In order to control the structure of membrane skin and to improve gas transport properties, the irradiation conditions, such as the dosage and the source of ion beams, have been varied. The ideal separation factor of CO2 over N2 through the surface-modified PI and PSf membranes increased threefold compared to those of the untreated, pristine membranes, whereas the permeability decreased with almost two orders of magnitude. This appears to be due to the fact that the structure of membrane skin has been changed to a barrier layer. The formation of barrier layer was confirmed by comparing the calculated values of a simple resistance model with the experimental results, and the estimated permeability of this barrier was 10−4 barrer. It was concluded that ion beam irradiation could provide a useful tool for improving selectivity for gas separation membranes.