• Bulletin of the Korean Chemical Society
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• 제23권8호
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• pp.1144-1148
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• 2002

We prepared the polyaniline (Pani) film and powder by chemical polymerization and doping with different dopants and also investigated the capability of Li//polyaniline cells after assembling. The oxidation/reduction potentials and electrochemical reaction of Li//polyaniline cells were tested by cyclic voltammetry technique. The Li//Pani-HCl cells with 10% and 20% conductors show a little larger specific discharge capacities than that without conductor. The highest discharge capacity of almost 50 mAh/g at 100th cycle is also achieved. However, Li//Pani-LiPF6 with 20% conductor shows a remarkable performance of ~90 mAh/g at 100th cycle. This is feasible value for using as the positive electrode material of lithium ion secondary batteries. It is also proved that the powder type electrode of Pani is better to use than the film type one to improve the specific discharge capacity and its stability with cycle.

• BMB Reports
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• 제47권7호
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• pp.376-381
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• 2014

Enzymatic oxidation of pyrogallol was efficiently transformed to an oxidative product, purpurogallin (PPG). Here, the anticoagulant activities of PPG were examined by monitoring activated partial thromboplastin time (aPTT), prothrombin time (PT), and the activities of thrombin and activated factor X (FXa). And, the effects of PPG on expression of plasminogen activator inhibitor type 1 (PAI-1) and tissue-type plasminogen activator (t-PA) were evaluated in tumor necrosis factor (TNF)-${\alpha}$ activated human umbilical vein endothelial cells (HUVECs). Treatment with PPG resulted in prolonged aPTT and PT and inhibition of the activities of thrombin and FXa, as well as inhibited production of thrombin and FXa in HUVECs. In addition, PPG inhibited thrombin-catalyzed fibrin polymerization and platelet aggregation. PPG also elicited anticoagulant effects in mice. In addition, treatment with PPG resulted in significant reduction of the PAI-1 to t-PA ratio. Collectively, PPG possesses antithrombotic activities and offers a basis for development of a novel anticoagulant.

• 한국환경보건학회지
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• 제31권4호
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• pp.241-245
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• 2005

Laccase catalyzes the oxidation and polymerization of aromatic compounds in the presence of molecular oxygen. Studies were conducted to characterize the use of polyethylene glycol (PEG) as an additive to keep up the enzymatic stability. The enzymatic activities highly remained and bisphenol A (BPA) was rapidly converted in the presence of 5 mg/l of PEC. These effects were accomplished with PEG of molecular weight 3,350. A linear relationship was found between the quantity of BPA to be converted $(10-120\;{\mu}M)$ and the optimum dose of PEC required for greater than $95\%$ conversion. This result suggests that it is the interaction between the PEG and the reaction products. In the optimum dose of PEG, the aeration of reaction mixture neither enhanced the conversion of BPA nor retarded the inactivation of the enzyme.

• 한국환경보건학회지
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• 제33권1호
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• pp.63-67
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• 2007

Laccase catalyzes the oxidation and polymerization of aromatic compounds in the presence of molecular oxygen. The oxidative transformation of chlorophene with laccase was conducted in a closed, temperature controlled system. The optimal pH for transformation of chlorophene was proven to be about 5-6. As the temperature rose up to $55^{\circ}C$, the transformation of chlorophene increased. The chlorophene transformation was not enhanced in the presence of soluble polymers. The toxicity of the reaction mixture was increased two times than that of initial reaction mixture after the enzymatic treatment. ABTS has enhanced chlorophene transformation at 0.1 mM and showed negative linear relationship with residual chlorophene by the reaction.

• Bulletin of the Korean Chemical Society
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• 제17권8호
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• pp.707-712
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• 1996

Growth and changes of electronically conducting polypyrrole (PPy) in the form of thin films polymerized on metal electrodes were investigated by electrochemical and in situ three-parameter ellipsometry methods at the wavelength of 632.8 nm. Although the optical equations produced multiple sets of solution, it was possible to determine a unique set of thickness and the optical constants of a film by auxiliary measurements and/or physical reasoning. The changes in the thickness and the optical properties of the polymers during polymerization and electrochemical oxidation/reduction was successfully followed by the three-parameter ellipsometric technique. The optical properties of the polymers continuously changed as the film grew. The imaginary part of the refractive index of polypyrrole seemed to be dominantly determined by the existence of an absorption band around the visible range.

• Bulletin of the Korean Chemical Society
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• 제9권4호
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• pp.248-251
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• 1988

Mechanism of electrochemical polymerization of pyrrole (Py) on a Pt electrode in acidic aqueous solutions was studied by means of potentiostatic measurements, cyclic voltammetry and chronopotentiometry. Pyrrole molecule appeared to be initially oxidized via two-electron transfer step to produce oxidized pyrrole ion ($Py^+$), which was coupled with a non-oxidized pyrrole to yield a dimerized species, Py-Py. The Py-Py thus formed was further oxidized again via two-electron transfer step, which was followed by coupling with non-oxidized monomer and by concomitant expulsion of a $H^+$. Then the latter chain extension process was repeated. The chain extension and polypyrrole oxidation reactions occurred competitively.

• 공업화학
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• 제16권1호
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• pp.86-92
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• 2005

아크릴 혼성 폴리우레탄 고분자의 열적-기계적 물성 및 내화학성 향상을 위해 프리폴리머 혼합 공정 및 무유화 중합을 통해 폴리(우레탄-에틸 아크릴레이트) 혼성 에멀젼을 합성하였다. 친수성 그룹의 도입을 위해 디메틸올 프로피온산을 사용하였으며, 폴리우레탄 프리폴리머 제조 후 프리폴리머에 에틸 아크릴레이트 단량체를 투입, 트리에틸 아민으로 증화시킨 후, 물에 분산시켜 안정한 에멀젼 액적을 형성하였다. 이 액적에 사슬 연장제인 에틸렌 디아민을 투입하여 폴리우레탄의 분자량을 증가시킨 후, 산화-환원 개시제인 t-BHP/SBS를 이용하여 $50^{\circ}C$에서 무유화 중합을 통해 폴리(우레탄-에틸 아크릴레이트) 혼성 에멀젼을 얻었다. 폴리(우레탄-에틸 아크릴레이트) 혼성 에멀젼의 물성(인장강도, 100% 모듈러스, 신율 및 내용제성)을 단독 폴리우레탄, 폴리(에틸 아크릴레이트) 및 단순 블렌딩에 의한 샘플과 비교 분석하였다.

• 대한화학회지
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• 제54권6호
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• pp.711-716
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• 2010

비닐렌기에 플루오르 치환기를 도입한 새로운 전자발광 (EL) 고분자인 poly(m-silylphenyl-p-phenylene-difluorovinylene) (m-SiP-PPDFV)는 GILCH polymerization 방법에 의해 합성된다. 이들 고분자는 단층 구조 (ITO/PEDOT/polymer/Ca:Al)의 light-emitting diodes (LEDs)에서 EL 발광층으로 사용되었다. m-SiP-PPDFV는 $\lambda_{max}$ = 452 nm 주위에서 PL 발광파장을 나타내었고, $\lambda_{max}$ = 497 nm 주위에서 녹색의 EL 발광을 나타내었다. 고분자의 current-voltage-luminance (I-V-L) 특성에서는 4.0 V 정도에서부터 소자가 작동되기 시작하였다. 고분자의 전자 친화도를 증가시키는 m-SiP-PPDFV을 얻기 위해 m-SiP-PPV의 모든 비닐렌기에 두개의 플루오르기를 도입하였고, 이로 인하여 소자 구동에서 비닐렌기의 색 안정도를 나타냈었다. PPV 유도체들에서 일어나는 비닐렌기의 산화반응을 보호하는 플루오르기는 전자 끄는 효과를 가지고 있어 소자의 색 안정도를 유지시킨다. 이번 연구로, 보다 안정화된 PPV 유도체를 얻기 위해, 플루오르기가 비닐렌기에 도입될 수 있음을 보여주고 있다.

• 한국재료학회지
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• 제23권5호
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• pp.276-280
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• 2013

Coal tar is the primary feedstock of premium graphitizable carbon precursor. Coal tars are residues formed as byproducts of thermal treatments of coal. Coal tar pitches were prepared through two different heat treatment schedules and their properties were characterized. One was prepared with argon and oxidation treatment with oxygen; the other was prepared with oxygen treatment at low temperature and then argon treatment at high temperature; both used coal tar to prepare coal tar pitches. To modulate the properties, different heat treatment temperatures ($300{\sim}400^{\circ}C$) were used for the coal tar pitches. The prepared coal tar pitches were investigated to determine several properties, such as softening point, C/H ratio, coke yield, and aromaticity index. The coal tar pitches were subject to considerable changes in chemical composition that arose due to polymerization after heat treatment. Coal tar pitch showed considerable increases in softening point, C/H ratio, coke yields, and aromaticity index compared to those characteristics for coal tar. The contents of gamma resin, which consists of low molecular weight compounds in the pitches and is insoluble in toluene, showed that the degree of polymerization in the pitches was proportional to C/H ratio. Using an oxidizing atmosphere like air to prepare the pitches from coal tar was an effective way to increase the aromaticity index at relatively low temperature.

• 폴리머
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• 제36권4호
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• pp.531-535
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• 2012

폴리아닐린(PANI) 나노섬유를 전도성 충전제로 사용하여 광경화형 전도성 투명필름을 제조하였다. 화학산화중합(chemical oxidation polymerization)으로 나노섬유 구조의 산화형 폴리아닐린(ES-PANI)을 합성하였다. ES-PANI는 디도핑을 통해 환원형 폴리아닐린(EB-PANI)으로 유도하였다. 이것을 전도성 충전제의 전구체로 사용하여 도데실벤젠설폰산(DBSA)이 포함되어 있는 광경화형 레진에 분산시키면 재도핑된 재산화형 폴리아닐린(rES-PANI)을 얻을 수 있었다. 이런 과정을 통해 나노섬유 형태가 유지되면서 높은 전도성과 분산안정성이 우수한 광경화형 전도성 레진용액을 제조할 수 있었다. 제조된 광경화형 전도성 레진용액은 상온에서 3달 정도 두어도 rES-PANI 충전제의 침전물이 생기지 않았다. 또한 이 용액을 폴리(메틸 메타크릴레이트)(PMMA) 기재 위에 스핀코팅 후 광경화하여 약 $5{\mu}m$ 두께의 전도성 투명필름을 제조하였다. rES-PANI 나노섬유 농도가 1.4 wt%일 때 표면저항 $6.5{\times}10^8{\Omega}/sq$, 550 nm 파장에서 91.1%의 투과도를 보였다. ES-PANI의 디도핑-재도핑(dedoping-redoping) 과정을 통해 광경화형 전도성 레진용액에 분산된 PANI는 농도에 따라 필름표면저항과 광학적 투명도를 조절할 수 있는 대전방지 보호필름을 제작하는 새로운 방법을 제시하였다.