• Applied Chemistry for Engineering
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• v.9 no.3
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• pp.342-347
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• 1998

Light-weight conductive polymer composites were prepared by incorporating polyheterocycles such as polypyrrole and polythiophene into pores of a highly porous cross-linked polystyrene, host polymer, to form a conductive network. The highly hydrophobic and porous host polymer was synthesized by concentrated emulsion polymerization method. Polypyrrole-based composites, prepared by employing ferric chloride-methanol system, showed a conductivity as high as 0.82 S/cm. Conductivity of polythiophene-based composites, prepared from ferric chloride-acetonitrile system, was 6.05 S/cm. Conductivity of compositivity was influenced by the initial molar ratio of oxidant to monomer as well. SEM micrographs of the composites showed that conducting polymer coated uniformly the inside wall of the porous host polymer. Shielding effectiveness of the polypyrrole-based composites and of the polythiophene-based composites were 15.2 dB and 22.5 dB at 2.0 GHz, respectively. In the temperature range from 20 to 300K, a polypyrrole impregnated composite exhibited seimiconducting behavior and followed the variable range hopping(VRH) model for charge transport.

• Membrane Journal
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• v.20 no.1
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• pp.21-28
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• 2010

Organic/inorganic composite electrolyte membranes were prepared for dye sensitized solar cell (DSSC). Poly (ethylene glycol) (PEG)s with various molecular weight (600, 1,500, 2,000 and 3,400) were ethoxysilated to fabricate organic/inorganic composite materials through sol-gel processes. The electrolyte membranes were produced by doping the composite materials with KI and $I_2$, and their ionic conducting behaviors were investigated. The ionic conductivity of the composite membrane was highly affected by PEG molecular weight. The highest conductivity was shown by the composite membrane prepared with PEG with the molecular weight of 2,000. The composite electrolyte membranes showed considerable improvement of ionic conductivity. Compared to PEO electrolyte membranes, the composite electrolyte membrane by PEG, MW 2,000 showed much higher ionic conductivity.

• Membrane Journal
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• v.20 no.2
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• pp.135-141
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• 2010

Various asymmetric Polysulfone membranes were prepared for a MBR process. Ether-typed alcohols (co-solvent) were added into a dope solution in order to control the pore size of membrane, whose effect on water permeability were investigated. Pore size of the prepared membranes were more affected by molecular-structure of co-solvent than by boiling point of theirs. With the increasing order of methoxy ($CH_3$-O-) < secondary propanol ($-CH_2$-CH(OH)$-CH_3$) < ethoxy ($CH_3-CH_2$-O-), water permeability of the prepared membrane increased. The phenomenon might attribute to the difference of molecularly steric hinderance of co-solvent (eg, Methoxy propanol, Ethoxy ethanol, Methoxy ethanol) in dope solution during the phase inversion. By the addition of ether typed alcohol into a dope solution, the pore size of MF (microfiltration) could be controlled. Also, Membrane prepared was applied to a MBR process and the system was stably operated for 2 months.

• Membrane Journal
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• v.18 no.4
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• pp.345-353
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• 2008

Organic/inorganic composite electrolyte membranes were prepared for dye sensitized solar cell (DSSC). Polyethylene Glycol (PEG)s with various molecular weight (400, 600, 1,500 and 3,400) was ethoxysilated to fabricate organic/inorganic composite materials through sol-gel processes. The electrolyte membranes were produced by doping the composite materials with NaI and $I_2$, and their ionic conducting behavior was investigated. The ionic conductivity of the composite electrolyte was highly affected by the PEG molecular weight, and the highest conductivity was shown by the composite membrane prepared with PEG with the molecular weight of 1,500. The composite electrolyte membranes showed considerable improvement of ionic conductivity. Compared to PEO electrolyte membranes, the composite electrolyte membrane prepared by PEG, MW 1,500, showed much higher ionic conductivity.

• Polymer(Korea)
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• v.24 no.1
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• pp.29-37
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• 2000

Polyaniline (PANi)/Poly(ethylene of oxide) (PEO) in-situ blends were prepared by inducing phase separation through solvent evaporation after casting from solutions containing aniline monomer, oxidant (initiator), dopant and PEO in methanol/water mixed solvent. It was observed that the electrical conductivity first increases rapidly as PANi amount in the PANi/PEO blend increases and then slowly increases as the weight percentages of polyaniline become above 11 wt% in the blend. We also noted that the morphology of PANi/PEO blends changes when the holding time in a stirrer at constant temperature is varied and eventually affects the electrical conductivity. As the length of alkyl group in dopants increases, the electrical conductivity of doped blends increases. The PANi/PEO blend prepared with a high molecular weight of PEO yields higher electrical conductivity.

• Polymer(Korea)
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• v.32 no.6
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• pp.587-592
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• 2008

High molecular weight poly(vinyl alcohol) (PVA) hydrogel to be expected as a candidate material for the wound-dressing was successfully prepared by electron beam (EB) irradiation. To produce PVA hydrogels with various gel fractions, degrees of swelling in water, gel strengths, and elongations, two different number-average degrees of polymerization [($P_n$)s] of PVA were adapted such as 1700 and 4000, and the PVA solution concentration and irradiation dose of EB were controlled to range of 5 $\sim$ 20% and 30 $\sim$ 100 kGy, respectively. The gel fraction and strength of PV A hydrogel were increased with increasing molecular weight of PVA, solution concentration, and irradiation dose of EB. On the contrary, the degree of swelling and elongation of PVA hydrogel were decreased. The thermal property and crystallinity related to degree of crosslinking of PVA hydrogel were examined by the analyses of differential scanning calorimetry and X-ray diffraction.

• Journal of the Korean Society of Food Science and Nutrition
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• v.29 no.4
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• pp.635-641
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• 2000

In order to utilize the protein source from a fish proessing by-product, cod was hydrolyzed with various enzymes such as tuna pyloric caeca crude enzyme (TPCCE), a-chymotrypsin, trypsin, papain and pronase E. The TPCCE hydrolysate acquired the highest sensory properties on taste, odor and color. The resultant cod rfame protein hydrolysate (CFPH) which was hydrolyzed with TPCCE, was separated through a series of ultrafiltration membranes with molecular weight cut-off (MWCO) of 30, 10, 5 and 1 kDa, and four types of permeates in cluding 30 K (permeate from 30 kDa membrane), 10 K (permeate from 10 kDa membrane), 5 K (permeate from 5 kDa membrane) and 1 K (permeate from 1 kDa membrane) were obtained. The natural sauces were prepared with 30 K, 10 K, 5 K and 1 K hydrolysate, and the sauce prepared with 1 K hydrolysate was the best score in sensory evaluations. In addition the mixed sauce prepared with 1 K hydrolysate and commercial soy sauce was similar to commercial sauce in sensory properties. These results suggest that the mixed sauce would be utilized as the substitute of acid-hydrolysis sauce.

• Proceedings of the Korean Fiber Society Conference
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• 2003.04a
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• pp.173-176
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• 2003

Poly(vinyl alcohol)(PVA)는 친수성이 좋고, 제조가 용이하며, 화학 약품에 대한 내성이 강한 특성을 가지고 있어, 코팅제나 페인트, 접착제 등 산업 전반에 널리 사용되고 있으며 섬유 제조에 대해서도 최근 활발하게 연구되고 있다. 전기방사(Electrospinning)는 전기장 내의 전위차를 이용하여 sub-micron 또는 nano-scale의 직경을 가지는 초극세 섬유를 제조할 수 있는 유용한 방법이다. (중략)

• Proceedings of the Korean Fiber Society Conference
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• 2003.04a
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• pp.372-373
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• 2003

전기방사는 고분자 용액에 전기장을 이용하여 나노섬유를 제조하는 유용한 방법이다. 전기방사에 의한 섬유 제조에 영향을 주는 공정인자들로는 고분자의 성질과 분자량 그리고 용액의 농도와 점도, 용매, 전기장의 세기, 콜렉터와의 거리에 의존한다[1-3]. TiO$_2$-SiO$_2$ 나노구조는 광학성, 열안정설, 내화학성 그리고 낮은열팽창성이 우수하여 반투명 코팅재, 광학센서, 광학유리, 보강재, 촉매재 등 광범위하게 응용될 수 있다. (중략)

• Proceedings of the Korean Fiber Society Conference
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• 1998.10a
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• pp.469-472
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• 1998

상업적으로 유용한 대부분의 합성고분자막들은 상전환법(phase inversion process)이라는 방법에 의해서 제조된다. 이 제조공정에서는 단일 고분자(homogeneous polymer)용액에 존재하는 용매를 비용매와 교환함으로써 액체로부터 고체로 상이 전환된다. 그리고 pore의 크기나 pore의 크기분포와 같은 막의 구조를 결정하는 요인은 일반적으로 용질의 입자크기 또는 분자크기 및 화학적 성질에 기인한다[1-3]. (중략)