• Membrane and Water Treatment
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• v.5 no.1
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• pp.41-56
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• 2014

A series of microporous PVDF membranes were prepared by isothermal immersionprecipitation of PVDF/TEP casting dopes in both soft and harsh coagulation baths. Morphologies of the membranes' top surfaces were found to depend strongly on the bath strength, which could be controlled by the TEP content in the bath. By changing the bath gradually from pure water to 70% TEP, the top surface evolved from a dense skin-like (asymmetric) to a totally open porous morphology (symmetric). The latter structure could similarly be obtained by precipitation of the same dope in an alcoholic bath, e.g., 1-butanol. Membrane distillation processes to desalt sodium chloride aqueous solutions were conducted using various prepared membranes and two commercial microporous membranes, PTFE (Toyo, Japan, code: J020A330R) and PVDF (GE, USA, code: YMJWSP3001). The permeation fluxes were compared and correlated with the morphologies of the tested membranes.

• Proceedings of the Membrane Society of Korea Conference
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• 1993.04a
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• pp.25-27
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• 1993

Multiphase equilibrium-based processes for separation and purification generally utilize dispersed systems in which one phase is dispersed in the other as bubbles or drops or thin films. Using microporous membranes, novel techniques have been developed such that multiphase processes can now be carried out in a nondispersive fashion for gas-liquid (Sirkar, 1992) and liquid-liquid (Prasad and Sirkar, 1992) contacting processes. Among such processes, only nondispersive solvent extraction of pollutants using microporous membranes will be of concern here. These processes employ immobilized immiscible phase interfaces at the pore mouths in a microporous membrane. Through such interfaces, solutes are extracted into the solvent as two immiscible phases flow on two sides of a microporous membrane. Many advantages of such a technique over conventional dispersion-based extractors have been summarized (Prasad and Sirkar, 1992).

• Membrane Journal
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• v.7 no.1
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• pp.1-10
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• 1997

A review is presented for various gas transport mechanisms through microporous membranes of both polymeric and inorganic materials. Different transport modes manifest depending on the pore size and the flow regime, which is a function of pressure, temperature, and the interaction between gas molecules and the pore walls. For microporous membranes whose pores are small and the internal surface area huge, the surface diffusion becomes a significant factor. If the pores become even smaller, then the transport mechanism will be more of an activated diffusion type. When conditions are right capillary condensation will take place to create an enormous capillary pressure gradient, which will greatly enhance the permeation flux. At the same time the capillary condensate of the heavier component may block the membrane pores denying the passage of the lighter gas molecules. All of these phenomena will influence the separation of mixtures.

• Proceedings of the Membrane Society of Korea Conference
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• 1995.09a
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• pp.1-13
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• 1995

A review is presented for various gas tranport mechanisms through microporous membranes of both polymeric and inorganic materials. Different transport modes manifest depending on the pore size and the flow regime, which is a function of pressure, temperature, and the inateraction between gas molecules and the pore walls. For microporous membranes whose pores are small and the intenal surface area huge, the surface diffusion becomes a significant factor. If the pores become even smaller, them the transport mechanism will be more of an activated diffusion type. When conditions are right capillary condensation will take place to create an enormous capillary pressure gradient, which will greatly enhance the permeation flux. At the same time the capillary condensate of the heavier component may block the membrane pores denying the passage of the lighter gas molecules. All of these phenomena will influence the separation of mixtures.

• Korean Membrane Journal
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• v.9 no.1
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• pp.1-11
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• 2007

To prepare chemically stable asymmetric microporous membranes with a hydrophilic surface, which would be expected to have better antifouling properties, poly(vinylidene fluoride) (PVDF) blend membranes were prepared by the phase inversion process. PVDF mixture solutions in N-methylpyrrolidone (NMP) blended with several polar potential ionic polymers such as polyacrylonitrile (PAN), poly(methylmethacrylate) (PMMA) and poly(N-isopropylacrylamide) (NIPAM) were used for the formation of the PVDF blend membranes. They were then characterized with several analytical methods such as FESEM, FTIR, contact angle measurement, pore size distribution and permeability measurement. Regardless of different polar polymers blended, they all showed a finger-like structure with more hydrophilic surface than the pristine PVDF membrane. For all the PVDF blend membrane, due to the polar potential ionic polymers used, the flux of those was improved. Especially the PVDF blend membrane with NIPAM showed the highest flux among the membranes prepared. Also antifouling property of the PVDF membrane was improved by the use of the polar polymers.

• Proceedings of the Membrane Society of Korea Conference
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• 1993.06a
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• pp.1-29
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• 1993

막 분리는 막의 물리화학적 특성, 분리대상 물질의 물리화학적 특성, 그리고 물질의 이동현상을 조절하는 압력차, 농도차 및 전위차 등의 추진력, 이 세가지 요소의 조합에 의해 행해진다. 막은 막을 구성하고 있는 물질의 물성, 구조, 막의 응용분야 및 역할 등에 의하여 세공막(Macroporous membranes), 미세공막(Microporous membranes), 비공성막(Nonporous membranes)등으로 분류된다.

• Proceedings of the Membrane Society of Korea Conference
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• 1998.06a
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• pp.135-153
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• 1998

Nanofiltration (NF) is a recently introduced term in membrane separation. In 1988, Eriksson was one of the first authors using the word 'nanofiltration' explicitly. Some years before, FilmTech started to use this term for their NF50 membrane which was supposed to be a very loose reverse osmosis membrane or a very tight ultrafiltration membrane. Since then, this term has been introduced to indicate a specific boundary of membrane technology in between ultrafiltration and reverse osmosis. The application fields of the NF membranes are very broad as follows: Demeneralizing water, Cleaning up contaminated groundwater, Ultrapure water production, Treatment of effleunts containing heavy metals, Offshore oil platforms, Yeast production, Pulp and paper mills, Textile production, Electroless copper plating, Cheese whey production, Cyclodextrin production, Lactose production. The earliest NF membrane was made by Cadotte et al, using piperazine and trimesoyl chloride as monomers for the formation of polyamide active layer of the composite type membrane. They coated very thin interfacially potymerized polyamide on the surface of the microporous polysulfone supports. The NF membrane exhibited low rejections for monovalent anions (chloride) and high rejections for bivalent anions (sulphate). This membrane was called NS300. Some of the earliest NF membranes, like the NF40 membrane of FilmTech, the NTR7250 of Nitto-Denko and the UTC20 and UTC60 of Toray, are formed by a comparable synthesis route as the NS300 membrane. Commercially available NF membranes nowadays are as follows: ASP35 (Advanced Membrane Technology), MPF21; MPF32 (Kiryat Weizmann), UTC20; UTC60; UTC70; UTC90 (Toray), CTA-LP; TFCS (Fluid Systems), NF45; NF70 (FilmTec), BQ01; MX07; HG01; HG19; SX01; SX10 (Osmonics), 8040-LSY-PVDI (Hydranautics), NF CA30; NF PES 10 (Hoechst), WFN0505 (Stork Friesland). The typical ones among the commercially available NF membranes are polyamide composite membrane consisting of interfacially polymerized polyamide active layer and microporous support. While showing high water fluxes and high rejections of multivalent ions and small organic molecules, these membranes have relatively low chemical stability. These membranes have low chlorine tolerance and are unstable in acid or base solution. This chemical instability is appearing to be a big obstacle for their applications. To improve the chemical stability, we have tried, in this study, to prepare chemically stable NF membranes from PVA. The ionomers and interfacially polymerized polyamide were used for the modification of'the PVA membranes. For the detail study of the active layer, homogeneous NF membranes made only from active layer materials were prepared and for the high performance, composite type NF membranes were prepared by coating the active layer materials on microporous polysulfone supports.

• Journal of the Korean Ceramic Society
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• v.23 no.5
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• pp.93-101
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• 1986

Microporous glasses were prepared from the 50 $SiO_2-44$ $B_2O_3-6$ $Na_2O$(wt%) parent glass by the phase eparation technique and were characterized by SEM, BET, and Gas Adsorption methods to investigate the possiblity of their use as salt-rejection membranes for reverse osmosis. The conditions of the phase separation for the possible glass membranes were optimized for the given parent glass. The temperature and duration of heat-treatment were desired to be lower(853K) and shorter (1/2~1 hr) respectively. The specific surface areas of porous glasses prepared in this study were about 80~120$m^2$/g and their pore size distribution had a unimodal shape(peak pore radius less than 15$\AA$) It was suggested that the porous glass obtained in this work could be effective for salt-rejection in point of pore size distributions but the way to increase its surface area for the high flux must be studied.

• Polymer Science and Technology
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• v.2 no.2
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• pp.81-87
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• 1991

• Membrane Journal
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• v.24 no.4
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• pp.317-324
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• 2014

It is very well known that the conventional polyamide (PA) thin film composite (TFC) reverse osmosis (RO) membranes have excellent permselective properties, but their chlorine tolerance is not good enough. In this study, to improve such chlorine tolerance, microporous membranes containing hydrophilic functional groups such as -COOH were used as a support to prepare PA TFC RO membranes, employing the conventional interfacial polymerization method. Meta-phenylene diamine (MPD) and 2,6-diamine toluene (2,6-DAT) were used as diamine monomers and tri-mesoyl chloride (TMC) as an acid monomer. The membranes prepared were characterized using various instrumental analytical methods and permeation test set-up. The flux obtained from the membranes prepared so was more than $1.0m^3/m^2day$ at 800 psi of operating pressure, while the salt rejection was over 99.0%. The chlorine tolerance of them was also found to be better than that of the membrane prepared by using conventional polysulfone support without hydrophilic functional groups.