• Applied Chemistry for Engineering
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• v.9 no.7
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• pp.979-984
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• 1998

The conducting composites were prepared by blending of polyaniline(PANI) as conducting polymer and nylon6,6 as matrix in m-cresol. The PANI was protonated with alkylbenzenesulfonic acid such as camphorsulfonic acid(CSA) or dodecylbenzenesulfonic acid(DBSA). The miscibility of the composites was improved and the electrical conductivity was increased by adding dioctylphthalate(DOP). The electrical conductivity of the composites depending on the amount of protonating agent and PANI complex and the morphology were investigated. When it was protonated with DBSA having long alkyl chain and the content of PANI complex was 25 wt%, the electrical conductivity of the compsosite was increased up to 1.02 S/cm.

• Journal of Advanced Marine Engineering and Technology
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• v.18 no.2
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• pp.54-63
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• 1994

Mg thin films were prepared on SPCC(cold-rolled steel) substrates by vasuum evapoaration and ion-plating. The influence of argon gas pressure and substrates bias voltage on the crystal orientation and morphology of the film was determined by using X-ray diffraction and scanning electron micrography (SEM), respectively. And the effect of crystal orientation and morphology of the Mg thin films on corrosion behavior was estimated by measuring the anodic polarization curves in deaerated 3% NaCl solution. The crystal orientation of the Mg films deposited at high argon gas pressure exhibited a (002) preferred orientation, regardless of the substrate bias voltage. Film morphology changed from a columnar to a granular structure with the increase of argon gas pressure. The morphology of the films depended not only on argon gas pressure but also bias voltage ; i.e., the effect of increasing bias voltage was similar to that of decreasing argon gas pressure. The influences of argon gas pressure and bias voltage were explained by applying the adsorption inhibitor theory and the sputter theory. And also, this showed that the corrosion resistance of the Mg thin films can be changed by controlling the crystal orientaton and morphology.

• Applied Chemistry for Engineering
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• v.10 no.6
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• pp.923-928
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• 1999

Polycarbonate(PC)/polypyrrole(PPy) conducting composites were prepared by precipitation polymerization. $FeCl_3$, pyrrole and chloroform were used as oxidant, monomer, and solvent, respectively. The electrical conductivity was increased with increasing the amount of PPy, while the mechanical property was decreased. When the PPy content was 25 wt %, the electrical conductivity of the composites was increased up to 0.23 S/cm. The electrical conductivity, the stability of conductivity in air and mechanical properties of the composites of different PPy content were investigated and the morphology of the composite films was observed.

• Applied Chemistry for Engineering
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• v.10 no.2
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• pp.287-292
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• 1999

The conducting composites were prepared by solution blending of polyaniline (PANI) as a conducting polymer and polycarbonate (PC) as a matrix in chloroform. Also the composites film was prepared by solution casting method. The PANI was protonated with alkylbenzenesulfonic acids, such as camphorsulfonic acid (CSA) or dodecylbenzenesulfonic acid (DBSA). The electrical conductivity of composites prepared by solution casting was enhanced compared with that of compression molding. The electrical conductivity, tensile strength and morphology were observed as a function of the amount of protonating agent as well as PANI complex content. In general, as the PANI complex content was increased, the electrical conductivity increased. In the case of the composite film containing 25 wt % of PANI complex doped with DBSA, the electrical conductivity exhibited 3.18 S/cm.

• Applied Chemistry for Engineering
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• v.10 no.2
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• pp.281-286
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• 1999

The conducting composites were prepared by blending polypyrrole (PPy) as a conducting polymer and nylon6,6 as a matrix. In chemical polymerization of PPy, the oxidizing agent was $FeCl_3$ and dopant was alkylbenzenesulfonic acid, such as camphorsulfonic acid (CSA) or dodecylbenzene sulfonic acid (DBSA). The electrical conductivity and mechanical properties were measured for the amount of dopant and PPy complex, and these morphology observed. When it was doped with DBSA having long alkyl chain and added the PPy complex of 25 wt %, the electrical conductivity was increased up to 0.64 S/cm.

• Proceedings of the Korean Institute of Surface Engineering Conference
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• 2012.05a
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• pp.275-275
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• 2012

실용금속 중 가장 경량이고, 치수 안정성, 절삭성 등이 우수한 Mg과 각종 산업의 구조물, 전기전자 부품 등의 분야에서 방식용 코팅 제품으로 많이 사용되고 있는 Zn를 혼합박막으로 Zn-Mg 박막을 제작하였다. 또한 여기서는 모재와 Zn-Mg 박막 사이에 결합력 강화를 위하여 Al중간층을 삽입하고 (Zn-Mg)/Al 박막을 제작하였다. 이와 같이 혼합박막을 제작하는 것은 Zn, Mg, Al 등과 같은 단일박막의 밀착성과 내식성의 한계를 극복-향상시키기 위한 것이었다. 한편, 이와 유사한 혼합박막에 많이 사용되고 있는 희생양극의 성분적인 측면이나 구조적인 분석에 있어서는 연구의 진척이 많이 이루어지고 있지만, 밀착성과 내식성의 상관관계의 규명에 있어서는 기초 단계이다. 따라서 본 연구에서는 여러 가지 증착 조건에 따라 제작한 막에 대한 표면 몰포로지, 결정배향성, 밀착성과 내식성에 미치는 영향을 분석하여 이들의 상관관계를 규명함은 물론 Al 중간층의 유무에 따른 서로간의 특성을 분석하였다. 분석결과에 의하면 Zn, Mg, Al 단일박막과 Zn-Mg 혼합박막에 비해 Al 중간층을 삽입한 (Zn-Mg)/Al이 내식성은 물론 밀착성이 우수하게 나타났다.

• Proceedings of the Korean Institute of Surface Engineering Conference
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• 2014.11a
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• pp.38-38
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• 2014

SPCC강판상에 PVD 스퍼터링법으로 Zn계 박막을 제작하였고, Zn계 박막의 결정구조와 표면특성에 미치는 산소의 영향을 해석하였다. 실험결과, 진공쳄버 내부에 있는 대부분의 Zn 이온중에서 Mg 이온이 증가할 때, Mg의 증발 및 흡착으로 인한 Zn의 증착핵 성장 억제와 Zn-Mg 금속간 화합물의 분산분포는 Zn-Mg막의 결정입자의 크기를 작게 만들었다. 산소가 쳄버내부에 존해하는 경우에는 XRD 피크는 상대적으로 감소되면서 브로딩하게 나타났다. 또한, 표면특성인 몰포로지의 경향을 분석해 보면 결정입도는 작아지는 현상을 보였다. 이것은 챔버 내부에 존재하는 잔류가스인 산소가 Zn 및 Mg과 같은 증착입자와 결합 및 흡착이 이루어지고, Zn 및 Mg 등이 증착핵의 마이그레이션 효과를 감소시켜 결정입도의 크기가 감소되는 것으로 나타났다.

• Journal of Advanced Marine Engineering and Technology
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• v.20 no.5
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• pp.103-113
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• 1996

The properties of the deposited film depend on the deposition condition and these, in turn depend critically on the morphology and crystal orientation of the films. Therefore, it is important to clarify the nucleation occurrence and growth stage of the morphology and orientation of the film affected by deposition parameters, e.g. the gas pressure and bias voltage etc. In this work, magnesium thin flims were prepared on cold-rolled steel substrates by a thermo-eletron activation ion plating technique. The influence of nitrogen gas pressure and substrate bias voltage on their crystal orientation and morphology of the coated films were investigated by scanning electron microscopy (SEM) and X-ray diffraction, respectively. The diffraction peaks of magnesium film became less sharp and broadened with the increase of nitrogen gas pressure. With an increase in nitrogen gas pressure, flim morphology changed from colum nar to granular structure, and surface crystal grain-size decreased. The morphology of films depended not only on gas pressure but also on bias voltage, i.e., the effect of increasing bias voltage was similar to that of decreasing gas pressure. The effect of crystal orientation and morphology of magnesium films on corrosion behaviors was estimated by measuring anodic polarization curves in deaerated 3%NaCl solution. Magnesium, in general, has not a good corrosion resistance in all environments. However, these magnesium films prepared by changing nitrogen gas pressure showed good corrosion resistance. Among the films, magnesium films which exhibited granular structure had the highest corrosion resistance. The above phenomena can be explained by applying the effects of adsorption, occlusion and ion sputter of nitrogen gas.

• Elastomers and Composites
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• v.46 no.4
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• pp.343-351
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• 2011

We prepared polyurethane foam/cloisite30B/phosphates composites and characterized their rise time, density, cell morphology, and thermal properties. The composites were synthesized with polyadipatediol-cloisite30B composite (f=2.0), polyether-polyol (f=4.6), polymeric 4,4-diphenyl methane diisocyanate (f=2.5), and D-580 (phenyl polyoxyalkenyl phosphate). As a blowing agent, cyclopentane and distilled water were used at various concentrations of D-580 from 0 to 2.81 wt%. The rise times of PUF/Closite30B/Phosphate composites blown with distilled water were faster than those blown with cyclopentane by 30%. The composites blown with cyclopentane had spherical-shape cells and the cell diameter was decreased with increasing D-580 wt%. While $T_g$ of the composites blown with cyclopentane linearly decreased with increasing the D-580 content, the $T_g$ of the composites blown with distilled water increased with the D-580 content. All PUF/Closite30B/Phosphate composites began to decompose from $250^{\circ}C$. The composites blown with cyclopentane showed the second thermal decomposition at temperatures higher than $500^{\circ}C$. The thermal stability of all composites increased with the D-580 content. The effect of D-580 on the thermal stability of the composites was measured higher at the composites blown with distilled water.