• 전기학회논문지
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• 제60권11호
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• pp.2088-2092
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• 2011

The accelerated thermal aging of CSPE(chloro sulfonate polyethylene) of test cables were carried out for the period equal to 10, 20 and 30 years in air at $100^{\circ}C$, respectively. The CSPE cables(TAIHAN electric wire Co. Ltd) which installed in nuclear power plant for three years were used as starting materials. Condition monitering methods of the accelerated thermal aging of CSPE cables were estimated through indenter modulus and OIT(oxidation induction time) of IEC 62582, and those were newly estimated through volume electrical resistivity, ultrasound reflection time, density, FE-SEM(field emission scanning electron microscopy), XPS(x-ray photoelectron spectroscopy), EDS(energy dispersive spectroscopy), and WD-XRF(wavelength dispersive x-ray fluorescence). A new condition monitoring methods of the accelerated thermal aging of CSPE cables were generally coincident with trend of indenter modulus expect EDS, XPS and XRF. A volume electrical resistivity among new condition monitoring methods of the accelerated thermal aging of CSPE cables is excellent. It is considered that life-time of CSPE cable can be predicted through volume electrical resistivity, if CSPE jacket was aged for period such as more than 20 years.

• Journal of Electrical Engineering and Technology
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• 제4권1호
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• pp.118-122
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• 2009

Organic thin film transistors with a pentacene active layer and various polymer gate insulators were fabricated and their performances were investigated. Characteristics of pentacene thin film transistors on different polymer substrates were investigated using an atomic force microscope (AFM) and x-ray diffraction (XRD). The pentacene thin films were deposited by thermal evaporation on the gate insulators of various polymers. Hexamethyldisilazane (HMDS), polyvinyl acetate (PVA) and polymethyl methacrylate (PMMA) were fabricated as the gate insulator where a pentacene layer was deposited at 40, 55, 70, 85, 100 oC. Pentacene thin films on PMMA showed the largest grain size and least trap concentration. In addition, pentacene TFTs of top-contact geometry are compared with PMMA and $SiO_2$ as gate insulators, respectively. We also fabricated pentacene TFT with Poly (3, 4-ethylenedioxythiophene)-Polysturene Sulfonate (PEDOT:PSS) electrode by inkjet printing method. The physical and electrical characteristics of each gate insulator were tested and analyzed by AFM and I-V measurement. It was found that the performance of TFT was mainly determined by morphology of pentacene rather than the physical or chemical structure of the polymer gate insulator

• 한국안전학회지
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• 제18권4호
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• pp.78-84
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• 2003

Core-shell composite particles of organic/organic were polymerized by using monomers such as methyl methacrylate(MMA) and styrene(St) in the presence of sodium dodecyl benzene sulfonate (SDBS) below critical micelle concentration(CMC) changing concentration, kind of initiators, emulsifiers, addition method of monomers and speed of agitation. In the PMMA/PSt and PSt/PMMA core-shell polymerization, to suppress the generation of new particles and to minimize the coagulation during the shell polymerization, the optimum conditions were $1.45{\times}10^{-5}mol/L$ and $2.91{\times}10^{-5}mol/L$ at concentration of SDBS respectively. The optimum concentration of the other initiator was $1.58{\times}10^{-3}mol/L$ of ammonium persulfate(APS) for core polymerization and $4.0{\times}10^{-4}mol/L$ of APS for shell polymerization.

• 대한전기학회:학술대회논문집
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• 대한전기학회 2004년도 추계학술대회 논문집 전기물성,응용부문
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• pp.278-280
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• 2004

본 논문의 내용은 다중전극에 전기 중합한 전도성 고분자를 이용하여 약물을 결합한 후 전압 인가에 의한 선택적인 약물방출을 구현하는 것이다. Glass wafer에 anode와 cathode 전극을 제작하고 4개의 anode 전극면에 각각 전기중합으로 전도성 고분자막을 합성하였다. 양이온성 약물인 lidocaine을 결합할 수 있도록 피롤과 함께 도펀트로써 분자량이 큰 DBS를 사용하였으며 고분자막의 이온출입원리를 이용하여 약물을 결합하고 방출하였다. Cyclic voltammogram로부터 PPy(DBS) Polypyrrole (dodecylbenzene sulfonate) 전극의 산화 환원특성 및 전극면에 PPy(DBS) 막이 생성되기 위한 조건을 확인하였고, 그 결과를 토대로 PPy(DBS)막을 3전극 시스템과 Coulometry를 이용하여 전압을 인가하여 합성하였고, 합성전하량으로 부터 PPy(DBS)막의 두께를 알 수 있었다. Lidocaine의 결합 및 방출 시에도 정전압을 이용하였으며 약물의 방출 유무를 확인하기 위하여 UV spectrometer를 사용하였다. 다중전극에 PPy(DBS)막을 1.5um 두께로 합성한 후 lidocaine을 결합시키고 선택적으로 약물을 방출한 결과 각각의 PPy(DBS)막으로부터 $1.4{\sim}1.7mg$의 약물이 방출됨을 확인 할 수 있었다.

• 한국분말야금학회:학술대회논문집
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• 한국분말야금학회 2006년도 Extended Abstracts of 2006 POWDER METALLURGY World Congress Part 1
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• pp.487-488
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• 2006

Novel bisphenol-based wholly aromatic poly(ether sulfone-ketone) copolymer containing pendant sulfonate groups were prepared by direct aromatic nucleophilic substitution polycondensation of 4,4-difluorobenzophenone, 2,2'-disodiumsulfonyl-4,4'-fluorophenylsulfone (40mole% of bisphenol A) and bisphenol A. Polymerization proceeded quantitatively to high molecular weight in N-methyl-2-pyrrolidinone at $180^{\circ}C$. Organic-inorganic composite membranes were obtained by mixing organic polymers with hydrophilic $SiO_2$ (ca. 20nm) obtained by sol-gel process. The polymer and a series of composite membranes were studied by FT-IR, $^1HNMR$, differential scanning calorimetry (DSC) and thermal stability. The proton conductivity as a function of temperature decreased as $SiO_2$ content increased, but methanol permeability decreased. The nano composite membranes were found to posse all requisite properties; Ion exchange capacity (1.2meq./g), glass transition temperatures $(164-183\;^{\circ}C)$, and low affinity towards methanol $(4.63-1.08{\times}10^{-7}\;cm^2/S)$.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2007년도 추계학술대회 논문집
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• pp.420-421
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• 2007

본 연구에서는 유기물 발광 다이오드(OLED)의 효율을 향상시키기 위하여 버퍼층 역할을 하는 PEDOT:PSS (poly(3,4-ethylenedioxythiophene) : poly styrene sulfonate)의 공정조건을 확립하고 두께에 따른 전기적 광학적 특성을 조사하였다. PEDOT:PSS는 spin coating 방법으로 증착을 하였으며, 흘효과측정을 통하여 ITO기판과 유기버퍼층이 코팅된 기판의 전하운반체의 이동도와 전류-전압 특성을 조사하였다. 그리고 UV-vis spectrometer를 이용하여 광투과도, 굴절률, 밴드갭을 측정하였고 SEM을 이용하여 시료의 표면도 관찰하였다. 유기물 버퍼층(PEDOT:PSS)의 두께가 얇을수록 정공의 이동도가 향상됨을 알 수 있었다.

• Macromolecular Research
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• 제10권6호
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• pp.304-310
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• 2002

In a recent study by the same authors using a DMTA (Dynamic Mechanical Thermal Analyzer), it was found that the 4-aminobenzoic arid (ABA) molecules acted as either a neutralizing agent, or a plasticizer, or a filler, depending on the order of mixing of poly(styrene-co-styrenesulfonic acid) (PSSA), ABA, and NaOH. Subsequent to that study, we here pursued the same topic, i.e., the effect of the addition of CsOH (instead of NaOH) and ABA on the morphology of PSSA, but this time, by using a small-angle X-ray scattering (SAXS) technique. In line with the previous results, the present study with the SAXS technique verified that the order of mixing has a significant effect on the morphology of ionomers. In addition, with the SAXS data and the density values of the ionomers, we attempted to calculate both the number of sulfonate ionic groups per multiplet and the size of the multiplet of the ionomer.

• 펄프종이기술
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• 제46권5호
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• pp.51-60
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• 2014

To find a practical application approach of polyelectrolyte multilayering (PEM) on inorganic filler, we introduced PEM process without washing step and investigated the effect of shear condition on the washless PEM treatment of ground calcium carbonate (GCC). Washless multilayering on GCC was conducted under various shear conditions such as stirring, homogenization, and ultrasonication. Highly charged polyelectrolytes combination of polydiallyldimethylammonium chloride (PDADMAC) and poly sodium 4-styrene sulfonate (PSS) and low charged polyelectrolytes combination with cationic starch and anionic polyacrylamide (PAM) were compared. In the case of highly charged polyelectrolytes combination, shear conditions did not affect the zeta potential and the particle size of treated GCC. However, the modified GCC particles with low charged polyelectrolytes were more dispersed under higher shear condition while maintaining the zeta potential. In addition, GCC was successfully modified through laboratory inline washless polyelectrolyte multilayering system which consists of homogenizers and pumps.

• 한국표면공학회지
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• 제27권5호
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• pp.292-302
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• 1994

Alloy deposits of 80Sn-20Pb, electroplated on Cu-based leadframe alloy from an organic sulfonate bath were aged at $150^{\circ}C$ to form intermetallic phases between substrate and deposit, and effects of the deposit morphology, influenced by deposition conditions, on the fracture resistance of the 80Sn-20Pb deposit aged at $150^{\circ}C$ were examined. The growth rate of intermetallic compound layer on aging depended on the microstructure of deposit ; it was fastest in deposit formed using pulse current in bath without grain refining additive, but slowest in deposit formed using dc current in bath containing grain refining additive in spite of similar structure with equivalent grain size. The grain refining additive incorporated in electrodeposit appears to inhibit diffusion of atoms on aging, resulting in slow growth of intermetallic layer in the thickness direction but substantial growth in the lateral one. Density of surface cracks that were occurring when samples were subjected to the $90^{\circ}$-bending test increased with increasing the thickness of intermatallic layer on aging. For the same aged samples, the surface crack density of the sample electrodeposited from a bath containing the grain refining additive was the least due to the inhibiting effect of the additive incorporated into the deposit during electrolysis on atomic diffusion.

• Bulletin of the Korean Chemical Society
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• 제16권5호
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• pp.416-421
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• 1995

The approximate rates and stoichiometry of the reaction of excess lithium gallium hydride with selected organic compounds containing representative functional groups were examined under the standard conditions (diethyl ether, 0 $^{\circ}C)$ in order to compare its reducing characteristics with lithium aluminum hydride and lithium borohydride previously reported, and enlarge the scope of its applicability as a reducing agent. Alcohols, phenol, and amines evolve hydrogen rapidly and quantitatively. However lithium gallium hydride reacts with only one active hydrogen of primary amine. Aldehydes and ketones of diverse structure are rapidly reduced to the corresponding alcohols. Conjugated aldehyde and ketone such as cinnamaldehyde and methyl vinyl ketone are rapidly reduced to the corresponding saturated alcohols. p-Benzoquinone is mainly reduces to hydroquinone. Caproic acid and benzoic acid liberate hydrogen rapidly and quantitatively, but reduction proceeds slowly. The acid chlorides and esters tested are all rapidly reduced to the corresponding alcohols. Alkyl halides and epoxides are reduced rapidly with an uptake of 1 equiv of hydride. Styrene oxide is reduced to give 1-phenylethanol quantitatively. Primary amides are reduced slowly. Benzonitrile consumes 2.0 equiv of hydride rapidly, whereas capronitrile is reduced slowly. Nitro compounds consumed 2.9 equiv of hydride, of which 1.9 equiv is for reduction, whereas azobenzene, and azoxybenzene are inert toward this reagent. Cyclohexanone oxime is reduced consuming 2.0 equiv of hydride for reduction at a moderate rate. Pyridine is inert toward this reagent. Disulfides and sulfoxides are reduced slowly, whereas sulfide, sulfone, and sulfonate are inert under these reaction conditions. Sulfonic acid evolves 1 equiv of hydrogen instantly, but reduction is not proceeded.