• Macromolecular Research
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• v.15 no.6
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• pp.565-574
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• 2007

In this study, five representative, commercially available polymers, Ultem 1000 polyetherimide, Kapton polyimide, phenolic resin, polyacrylonitrile and cellulose acetate, were used to prepare pyrolyzed polymer membranes coated on a porous {\alpha}-alumina$ tube via inert pyrolysis for gas separation. Pyrolysis conditions (i.e., final temperature and thermal dwell time) of each polymer were determined using a thermogravimetric method coupled with real-time mass spectroscopy. The surface area and pore size distribution of the pyrolyzed materials derived from the polymers were estimated from the nitrogen adsorption/desorption isotherms. Pyrolyzed membranes from polymer precursors exhibited type I sorption behavior except cellulose acetate (type IV). The gas permeation of the carbon/{\alpha}-alumina$ tubular membranes was characterized using four gases: helium, carbon dioxide, oxygen and nitrogen. The polyetherimide, polyimide, and phenolic resin pyrolyzed polymer membranes showed typical molecular sieving gas permeation behavior, while membranes from polyacrylonitrile and cellulose acetate exhibited intermediate behavior between Knudsen diffusion and molecular sieving. Pyrolyzed membranes with molecular sieving behavior (e.g., polyetherimide, polyimide, and phenolic resin) had a $CO_2/N_2$ selectivity of greater than 15; however, the membranes from polyacrylonitrile and cellulose acetate with intermediate gas transport behavior had a selectivity slightly greater than unity due to their large pore size.

• Membrane Journal
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• v.32 no.5
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• pp.348-356
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• 2022

With the development of the bio industry, membrane chromatography with a high adsorption efficiency is emerging to replace the existing column chromatography used in the downstream processes of pharmaceuticals, food, etc. In this study, through the deacetylation reaction of two commercial cellulose acetate (CA) membranes with different pore sizes, the porous regenerated cellulose (RC) supports for membrane chromatography were obtained to attach the anion exchange ligands. The adsorptive membranes for anion exchange were prepared by attaching an anion exchange ligand ([3-(methacryloylamino) propyl] trimethylammonium chloride) containing quaternary ammonium groups on the RC supports by grafting and UV polymerization. The protein adsorption capacities of the prepared membranes were obtained through both the static binding capacity (SBC) and the dynamic adsorption capacity (DBC) measurement. As a result, the membrane chromatography with the smaller the pore size, the larger the surface area showed the highest protein adsorption capacity. Membrane chromatography which was prepared by using deacetylated commercial CA support with MAPTAC ligand (i.e., RC 0.8 + MAPTAC: 43.69 mg/ml, RC 3.0 + MAPTAC: 36.33 mg/ml) showed a higher adsorption capacity compared to commercial membrane chromatography (28.38 mg/ml).

• Proceedings of the Membrane Society of Korea Conference
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• 1998.10a
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• pp.120-122
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• 1998

현재 상업화되어있는 RO membrane으로는 크게 asymmetric membrane과 composite membrane으로 구분될 수 있다. Asymmetric membrane의 소재로는 Cellulose acetate나 Cellulose triacetate와 같은 것들이 사용되며 현재에도 많이 사용되고 있으나, 보다 더 우수한 성능을 갖는 분리막을 제조하기 위해 현재에는 주로 composite membrane 형태로 제조된다. 대부분의 composite membrane은 계면중합에 의해 제조되는데 대표적인 membranem으로는 FT-30이 있다. 이 밖에도 support의 표면을 직접 플라즈마 처리하여 복합막을 제조하는 공정이 있으며 polyactrylonitrile과 같은 membrane이 이에 속한다. 플라즈마 처리된 복합막은 처리 대상에 크게 영향을 받지 않고 support 표면에 crosslinking의 형태로 형성되기 때문에 active layer가 매우 안정하며 따라서 우수한 물리화학적 성질을 기대할 수 있다. 이밖에도 분리막 표면을 친수성 단량체로 플라즈마 처리함으로써 분리막 표면에 친수성을 부여하거나 관능기를 도입함으로써 불활성 표면을 활성화 시킬 수도 있는 등의 여러가지 장점을 가지고 있다.

• Membrane and Water Treatment
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• v.10 no.6
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• pp.441-449
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• 2019

In this study, cellulose acetate (CA) / nylon66 (NYL66) (95/5) blend membranes with different thicknesses were prepared by a solvent evaporation method. The effects of membrane thickness (almost $7-25{\mu}m$), feed concentration (70-95 wt.% isopropanol), and feed temperature ($30-60^{\circ}C$) were investigated on the performance of membrane in the separation of isopropanol-water mixtures. With regard to the results of sorption experiments, it was found that the increase of feed temperature enhanced the overall sorption while by increasing feed concentration, the overall sorption passed through a maximum value at 70 wt. % isopropanol (IPA). The best separation factor 3080.51 was gained at high isopropanol concentration 95 wt.%, low feed temperature $30^{\circ}C$, and high membrane thickness $24.62{\mu}m$. Regarding the pervaporation separation index, the obtained results showed that proper values for the thickness of membrane, feed temperature, and isopropanol concentration in feed were $24.62{\mu}m$, $40^{\circ}C$, and 70 wt.%, respectively.

• Membrane Journal
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• v.23 no.6
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• pp.425-431
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• 2013

This paper has studied the hydrophilizing effect of support on the performance of pressure retarded osmosis (PRO). The hydrophilicity of polyester support has been controlled with cellulose solutions. In order to investigate the effect of hydrophilizing of support, the performance test has been conducted with membrane which compose of active layer and support in absence of support layer. The active layer has been made by casting of cellulose tri-acetate (CTA) 1,4-dioxane solution (13 wt%) and combined with the hydrophilized support. The results show that water fluxes of PRO membranes with hydrophobic or hydrophilized support were measured $0.8L/m^2hr$ and $1.2L/m^2hr$ under $5kgf/cm^2$ pressure, respectively. However, water flux increase did not accord with hydrophilicity of supports treated by cellulose solutions. It is because the porosity and pore size of supports decrease as the cellulose concentration increases. This result confirms that both the hydrophilization of support and the maintenance of membrane porosity are important to enhance the performance of PRO membrane.

• 한국생물공학회:학술대회논문집
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• 2000.11a
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• pp.260-263
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• 2000

Membranes are widely used to separate target solute molecules such as proteins on the basis of their size in cell broth mixture to minimize the loss of target compounds. In this study, membrane separation system using ultrafilters of MWCO 100 K and 50 K, was operated for concentration and purification of microbial transglutaminase. Fermentation broth containing MTGase was prefiltered by using pore size 1.6 and $0.7\;{\mu}m$ pre-filter made of cellulose fiber and $0.45\;{\mu}m$ microfilter made of cellulose acetate. The prefiltered solution was concentrated by 100 K and 50 K ultrafilter. The final enzyme concentration was 1.29 units/ml and enzyme specific activity was 0.2 units/mg protein. This specific activity were 3.7 times higher than that of initial cell broth mixture. Membrane separation process of microfiltration and ultrafiltration was proved to be very economic, energy efficient and effective separation method used to concentrate MTGase.

• Nuclear Engineering and Technology
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• v.15 no.1
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• pp.1-10
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• 1983

By controlling both the means of grafting and the cast-solution components, no degradation and dimensional change of radiation-induced graft polymerization were found. The electric resistance of styrene-cellulose acetate grafts increases with increasing styrene content, while those for the hydrophilic monomers show no marked effect. In comparison with the grafted cellulose acetate membrane by simultaneous irradiation method, the appearance of the grafted membrane by post-polymerization method was not markedly changed irrespective of the percent of grafting and radiation dose of electron beam or ${\gamma}$-ray. The combination of crosslinking agents such as divinyl benzene (OB) or trimethyl propane triacrylate (TMPT) in the VP:St:BPO system leads to gradual increase of the percent of grafting. The activation energy for grafting of St:VP:BPO solution onto cellulose acetate membrane was determined to be about 21.8 Kcal/mole over the range of 55$^{\circ}$-8$0^{\circ}C$. The initial rate of grafting (in %/hr) is proportional to the power 0.76 for dose intensities.

• Membrane Journal
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• v.9 no.1
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• pp.17-24
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• 1999

Milk was concentrated by commercial tubular membranes, The permeation rate reduction of hydrophilic membranes (sulfonated poly sulfone (SPSf), polyacrylonitrile (PAN), cellulose acetate (CA)) was found not to be large but hydrophobic membranes to be pronounced considerably, In the case of UF concentration total solids, proteins, fats and minerals were increased as concentrated but carbohydrates decreased. NF showed the same behavior except carbohydrates showing small reduction rate.

• Membrane Journal
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• v.20 no.3
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• pp.222-227
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• 2010

The purpose of this study is to prepare forward osmosis (FO) membranes using a variety of cellulose-based polymers and to evaluate the performance of difference depending on each of the polymers and additives. Forward osmosis membranes based on cellulose acetate (CA) and cellulose triacetate (CTA) were prepared through phase inversion. The performance of FO membranes developed, such as flux and salt rejection, was compared under the osmotically- and pressure-driven conditions. In CA FO membranes, the execution time of solvent evaporation and membrane annealing induced the change in membrane performance. But the performance of CTA FO membrane was improved by using additives rather than annealing. Moreover, the flux of CTA FO membrane was $4.46\;L/m^2hr$ but that of CA/CTA FO membrane was $8.89\;L/m^2hr$ in FO mode. The CTA FO membrane with blending CA was more efficient to increase FO permeate flow rather than using a single polymer membrane.

• Membrane Journal
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• v.1 no.1
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• pp.55-64
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• 1991

The ultrathin membranes of cellulose acetate and polyvinyl chloride were prepared by the method of watercasting. The spreading ability of polymer solutions on water doereased with increasing the surface tention and the viscosity of polymer solutions, and the temperature of water surface, respectively. The aggregation states of water-casting membranes were dense and dense with increasing the concentration of polymer solutions and the temperature of water surface. The surface structure of the air sides showed more dense than that of the water sides. In the case of the 3 wt% cellulose acetate/acetone system, the thickness of the membrane was about $0.1{\mu}.$.