목적: 플라즈마 표면처리가 불화규소 아크릴레이트 재질의 RGP 콘택트렌즈의 물리화학적 특성에 미치는 영향을 분석하였다. 방법: RGP 렌즈 표면의 플라즈마 처리는 공기 중 상온에서 200 W로 수행하였으며, 처리시간은 0∼250초로 다르게 하였다. 습윤성을 평가하기 위해 접촉각을 측정하였다. 표면 성분은 X-선광전자분광분석기(XPS)로 관찰하고, 플라즈마 처리에 의한 실리케이트의 형성을 분석하였다. 표면의 형상과 거칠기는 원자현미경(AFM)으로 관찰하였다. 산소침투성의 변화는 전기분해 분석법으로 얻은 렌즈의 투과 전류값과 중심두께를 측정하여 비교하였다. 결과: 플라즈마로 표면 처리되면 초기에 접촉각이 급격히 감소하였으며, 처리되지 않은 표면에 비해 30%까지 감소하였다. 표면 성분의 탄소와 불소는 70% 이하로 감소했으나, 산소와 실리콘은 150% 이상 증가하였다. 표면에서 탄소가 감소하는 형태는 접촉각의 변화와 직접적으로 관계가 있었다. 플라즈마 표면처리에 의해 표면의 탄소와 불소는 휘발하고, 유리된 실리콘이 산소와 결합하여 표면에 친수성 실리케이트(SiOx, x=1.5∼2.0)가 형성되며, 실리케이트는 50% 이상 크게 증가하였다. 플라즈마 처리된 표면에서 원형이나 직각형의 돌출부가 관찰되고, 거칠기(RMS)는 40% 이상 증가하였다. 결론: RGP 콘택트렌즈를 공기 중에서 플라즈마 처리하면 표면에 친수성인 실리케이트가 형성되어 습윤성은 개선되지만 산소침투성에는 영향을 주지 않았다. 습윤성의 증가는 표면형상의 변화보다는 실리케이트의 형성이 더 큰 영향을 준 것으로 판단되었다. 또한 플라즈마 처리에 의해 표면에 국한되어 형성된 실리케이트가 열린 구조를 갖고 있어 산소침투성에 유의한 변화가 없었던 것으로 생각된다.

One of the most important characteristics of Mg alloys is the high ratio of strength to weight. This is why there is a high demand for applications with these alloys in the transportation industries to reduce the fuel consumption and to save energy. In addition, magnesium (and its alloys) is of considerable interest as a structural material, especially in the aerospace and automotive industries thanks to its low density. However, its major drawback is its high sensitivity to corrosion. Therefore, its use requires the application of a surface treatment. This study used a die-casted AZ91D Mg alloyand all the samples were annealed (in 120˚C). The surface microstructure and phase distribution in thin-walled AZ91D magnesium components cast on a hot-chamber die-casting machine were investigated by optical microscopy and scanning electron microscopy. The reflectance differences in the bulk state comparison with the annealing state are caused by hydrogenation presence of the Mg layer under an oxidation surface layer.

Recently, consumption of magnesium alloys has increased especially in the 3C (computer, communication, camera) and automobile industries. The structural application of magnesium alloys has many advantages due to their low densities, high specific strength, excellent damping and anti-eletromagnetic properties, and easy recycling. However, practical application of these alloys has been limited to narrow uses of mild condition, because they are inferior in corrosion resistance and wear resistance due to their high chemical reactivity and low hardness. Various wet and dry processes are being used or are under development to enhance alloy surface properties. Various conversion coating and anodizing methods have been developed in a view of eco-friendly concept. The conventional technologies, such as diffusion coating, sol-gel coating, hydrothermal treatment, and organic coating, are expected to be newly applicable to magnesium alloys. Surface treatments for metallic luster or coloring are suggested using the control of the micro roughness. This report reviews the recent R&D trends and achievements in surface treatment technologies for magnesium alloys.

목적: RGP 콘택트렌즈의 습윤성을 향상시키기 위한 플라즈마 처리의 효과가 얼마나 지속되는지 알아 보고, 렌즈를 착용했을 때 임상적인 성능을 평가하고자 하였다. 방법: 플라즈마 처리된 RGP 콘택트렌즈와 일반 RGP 콘택트렌즈를 세척하기 전과 6회 세척하는 동안 접촉각을 측정하였다. 세척할 때마다 자연건조 후 Sessile drop 방식으로 접촉각을 측정하였다. 세척제는 연마재가 첨가된 것과 연마재가 첨가되지 않은 것을 사용하였다. 대상자의 우안과 좌안에 무작위로 플라즈마 처리 RGP 콘택트렌즈와 일반 RGP 콘택트렌즈를 착용시켰다. 렌즈를 착용하고 있을 때 표면의 습윤성을 평 가하기 위해 렌즈 전면의 NIBUT와 NIDUT를 검사하였다. 결과: 플라즈마 처리된 RGP 콘택트렌즈는 일반 RGP 콘택트렌즈보다 초기 습윤성이 높았지만 세척 후 접촉각이 점차 증가되었다. 연마재가 첨가된 세척액을 사용하여 4회 세척했을 때와 연마재가 첨가되지 않은 세척액을 사용하여 6회 세척했을 때 일반 RGP 콘택트렌즈와 접촉각의 차이가 없었다. 렌즈 전면의 NIBUT 와 NIDUT는 착용1일째 플라즈마처리RGP 콘택트렌즈가일반 RGP 콘택트렌즈보다 더 높았으나 착용7일째에는 유의한 차이가 없었다. 결론: 플라즈마 처리 효과는 최대 1주일 정도 지속되고 초기 착용감을 향상시켜서 적응에 도움을 주는 것으로 판단된다.

MAO(Micro-Arc Oxidation) method was used to make surface on 6063 Al specimen. This study was focused on an influence of voltage, density of electrolyte and a period of treatment on the change of surface microstructure by using SEM(Scanning Electron Microscope), EDS(Energy Dispersive X-ray Spectroscopy). The microstructure shows higher roughness and thicker oxidized layer with increase of voltage and maintaining period of treatment. The density of electrolyte affected a formation of more dense surface and increase of a oxidized layer.

In preparation of silica aerogel-based hybrid coating materials, the combination of hydrophobic aerogel with organic polar binder material is shown to be very limited due to dissimilar surface property between two materials. Accordingly, the surface modification of the aerogel would be required to obtain compatibilized hybrid coating sols with homogeneous dispersion. In this study, the surface of silica aerogel particles was modified by using both surfactant adsorption and heat treatment methods. Four types of surfactants with different molecular weights and HLB values were used to examine the effect of chain length and hydrophilicity. The surface property of the modified aerogel was evaluated in terms of visible observation for aerogel dispersion in water, water contact angle measurement, and FT-IR analysis. In surface modification using surfactants, the effects of surfactant type and content, and mixing time as process parameter on the degree of hydrophilicity for the modified aerogel. In addition, the temperature condition in modification process via heat treatment was revealed to be significant factor to prepare aerogel with highly hydrophilic property.

Propellant waste was impregnated on the surface of activated carbon fiber and heat-treated at different temperature to introduce newly developed functional groups on the ACF surface. Functional groups of nitrogen and oxygen such as pyridine, pyridone, pyrrol, lacton and carboxyl were newly introduced on the surface of modified activated carbon fiber. The porosity, specific surface area, and morphology of those modified ACFs were changed as increasing the heat-treated temperature from 200 to 500℃. The optimum heat-treatment temperature was suggested to 500℃, because lower temperature given rise to the decrease of specific surface area and higher temperature resulted in the decrease of weight loss. Propellant waste can be used as an useful surface modifier to porous carbons.

In this work, the effect of aminized multi-walled carbon nanotubes (NH-MWNTs) on the mechanical interfacial properties of epoxy nanocomposites was investigated by means of fracture toughness, critical stress intensity factor (KIC), and impact strength testing, and their morphology was examined by scanning electron microscope (SEM). It was found that the incorporation of amine groups onto MWNTs was confirmed by the FT-IR and Raman spectra. The mechanical interfacial properties of the epoxy nanocomposites were remarkably improved with increasing the NH-MWNT content. It was probably attributed to the strong physical interaction between amine groups of NH-MWNTs and epoxide groups of epoxy resins. The SEM micrographs showed that NH-MWNTs were uniformly embed and bonded with epoxy resins, resulted in the prevention of the deformation and crack propagation in the NH-MWNTs/epoxy nanocomposites.

Low temperature degradation behavior in yttria stabilized tetragonal zirconia polycrystal (Y-TZP) ceramics was microscopically observed from the phase contrast between monoclinic surface and tetragonal matrix. The degradation behavior was dependent on the surface treatment of sintered Y-TZP, even if the sintering history is same. In the mirror polished specimen, the monoclinic layer appeared in a uniform thickness from the surface. On the contrary, for the specimen with coarse scratch, the thickness of degraded surface was more than double especially from the coarse scratch. Since the scratch results in local deformation, the residual stress should be induced around the scratch. With the transformation from tetragonal to monoclinic, the volume expansion exerts a stress on a neighboring grains and promotes a successive phase transformation. Such a autocatalytic effect can be triggered from the part of coarse scratch.

Recently, metal molding has become essential not only for automobile parts, but also mass production, and has greatly influenced production costs as well as the quality of products. Its surface has been treated by carburizing, nitriding and induction hardening, but these existing treatments cause considerable deformation and increase the expense of postprocessing after treatment; furthermore, these treatments cannot be easily applied to parts that requiring the hardening of only a certain section. This is because the treatment cannot heat the material homogeneously, nor can it heat all of it. Laser surface treatment was developed to overcome these disadvantages, and, when the laser beam is irradiated on the surface and laser speed is appropriate, the laser focal position is rapidly heated and the thermal energy of surface penetrates the material after irradiation, finally imbuing it with a new mechanical characteristic by the process of self-quenching. This research estimates the material characteristic after efficient and functional surface treatment using HPDL, which is more efficient than the existing CW Nd:YAG laser heat source. To estimate this, microstructural changes and hardness characteristics of three parts (the surface treatment part, heat affect zone, and parental material) are observed with the change of laser beam speed and surface temperature. Moreover, the depth of the hardened area is observed with the change of the laser beam speed and temperature.

The investigation is to modify the mechanical and chemical properties of Mg alloys using a combination of rapid solidification and surface treatment. As the first approach, was gas atomized and pressure sintered by spark plasma sintering process (SPS), showing much finer microstructure and higher strength than the alloys as cast. Further modification was performed by treating the surface of PM Mg specimen using Plasma electrolytic oxidation (PEO) process. During the PEO processing, MgO layer was initiated to form on the surface of Mg powder compacts, and the thickness and the density of MgO layer were varied with the reaction time. The thickening rate became low with the reaction time due to the limited diffusion rate of Mg ions. The surface morphology, corrosion behavior and wear resistance were also discussed

The objective of this paper is to compare the variation of surface properties by hydrochloric acid pre-treatment and of metallic potassium and their salts loading effect for activated carbon after surfaces transformation by acid. From the results of nitrogen adsorption, each isotherm shows a distinct knee band, which is closely related to the characteristic of microporous carbons with capillary condensation in micropores. In order to present the causes of the differences in surface properties and SBET after the samples were treated with hydrochloric acid, pore structure and surface morphology are investigated by adsorption analysis. X-ray diffraction (XRD) patterns indicate that activated carbons show better performance for metallic potassium and potassium salts by pre-treatment with hydrochloric acid. Scanning electron microscopy (SEM) pictures of potassium/activated carbon particles provide information about the homogeneous distribution of metal or metal complex on the surface. For the chemical composition microanalysis for potassium treatment of the activated carbon pre-treated with hydrochloric acid, samples were analyzed by energy disperse X-ray (EDX). Finally, the type and quality of oxygen groups are determined from the method proposed by Boehm. A positive influence of the acidic groups on the carbon surface by acid treatment is also demonstrated by an increase in the contents of potassium salts with increasing of acidic groups calculated from Boehm titration.

The objective of this study was to investigate the possibility of application for water treatment using the zeocarbon. The zeocarbon was mixture of zeolite and activated carbon. In general, the application of commercial zeocarbon to water treatment is difficult because of weak strength in water and the high pH value of effluents after water treatment. Therefore, we have modified the surface of zeocarbon. For the surface modification, we used the acid treatment to make surface functional group. As a result of modification, was created functional group on zeocarbon surface and was formed mesopore in zeocarbon. The surface modified zeocarbon was applied to removal of nitrogen. In removal experiments of nitrogen, removal efficiency was very high. And, strength of zeocarbon after water treatment and pH of effluents were stabilized. This indicates that the surface modified zeocarbon was easy to recover and reuse. Consequently, our results were shown the possibility of application for water treatment using the surface modified zeocarbon.

균일한 밀집구조를 지니는 투명한 폴리설폰 필름이 용매를 사용한 표면처리를 통해 개질되었다. 개질은 고분자 필름을 디메털포름아마이드 용매에 1 sec간 담그고 이를 비용매 욕조에 침지시켜 이루어졌다. 개질 전 투명하였던 필름은 개질 후 횐색을 띠며, 많은 기공이 표면에 형성되었다. 비용매로서 물을 사용하였을 때가 이소프로파놀을 사용하였을 때 보다 표면의 불균일도가 증가하였다. 개질된 필름을 사용하여 방사성핵종으로 오염된 지역으로부터 오염물을 채취하였을 때 일반적으로 사용되는 필터페이퍼를 사용하는 것보다 우수한 채취 효율을 보여주었다. 개질된 필름 중에서는 비용매로 물을 사용한 경우 이소프로파놀을 이용한 필름보다 오염물의 채취 효과가 좋은 것으로 나타났다. 한편, 개질된 필름은 고분자 필름의 양쪽 겉표면만을 변화시켜, 필름의 내부는 고유한 밀집도를 유지함으로써, 필터페이퍼 또는 유리섬유를 사용한 오염물 제거 과정에서 나타날 수 있는 매체의 기공을 통한 2차적 오염을 방지하는 효과가 있다.

The effects of fiber surface-treatment and sizing on the dynamic mechanical properties of unidirectional and 2-directional carbon fiber/nylon 6 composites by means of dynamic mechanical analysis have been investigated in the present study. The interlaminar shear strengths of 2-directional carbon/nylon 6 composites sized with various thermosetting and thermoplastic resins are also measured using a short-beam shear test method. The result suggests that different surface-treatment levels onto carbon fibers may influence the storage modulus and tan δ behavior of carbon/nylon 6 composites, reflecting somewhat change of the stiffness and the interfacial adhesion of the composites. Dynamic mechanical analysis and short-beam shear test results indicate that appropriate use of a sizing material upon carbon fiber composite processing may contribute to enhancing the interfacial and/or interlaminar properties of woven carbon fabric/nylon 6 composites, depending on their resin characteristics and processing temperature.