본 연구에서는 다양한 실내시험을 통하여 국내에서 개발된 에폭시 아스팔트 혼합물의 공용성을 평가하였다. 최대입경 13mm의 밀입도 혼합물을 기초로 하여 아스팔트 바인더의 20% 또는 40%를 국산 및 일본산 에폭시 수지로 치환하여 4종류의 에폭시 아스팔트 혼합물의 배합 설계를 실시하였다. 에폭시 아스팔트의 가사시간이 에폭시 수지가 40% 사용한 경우 3시간, 20% 사용한 경우 6시간 정도임을 확인할 수 있었다. 휠트랙킹 시험, 간접인장 반복시험, 그리고 저온 휨 시험 결과 국산 및 일본산 에폭시 아스팔트 혼합물의 공용성이 일반 아스팔트 혼합물 보다 상당히 우수한 것으로 나타났다. 하지만 일부 에폭시 아스팔트 혼합물에서는 수분손상 가능성을 확인할 수 있었다. 또한 일본산 에폭시 아스팔트 혼합물과 국산 에폭시 아스팔트는 유사한 성능을 나타냈다. 또한 콘크리트 보수재로 개발한 국산 에폭시 아스팔트의 적합성을 평가하기 위하여 추가적으로 열팽창계수, 부착강도, 인장강도를 측정한 결과, 일반 콘크리트와의 부착력은 우수하고 인장강도는 유사한 것으로 나타났으나 열팽창계수는 5배정도 큰 것으로 나타났다.

Carbon/epoxy woven composites are prominent wear-resistant materials due to the strength, stiffness, and thermal conductivity of carbon fabric. In this study, the effect of oilabsorption on the wear behaviors of carbon/epoxy woven composites was investigated. Wear tests were performed on dry and fully oil-absorbed carbon/epoxy woven composites. The worn surfaces of the test specimens were examined via scanning electron microscopy to investigate the wear mechanisms of oil-absorbed carbon/epoxy woven composites. It was found that the oil absorption rate was 0.14% when the carbon/epoxy woven composites were fully saturated. In addition, the wear properties of the carbon/epoxy woven composites were found to be affected by oilabsorption. Specifically, the friction coefficients of dry and oil-absorbed carbon/epoxy woven composites were 0.25-0.30 and 0.55-0.6, respectively. The wear loss of the oilabsorbed carbon/epoxy woven composites was 3.52×10-2 cm3, while that of the dry carbon/epoxy woven composites was 3.52×10-2 cm3. SEM results revealed that the higher friction coefficient and wear loss of the oil-absorbed carbon/epoxy woven composites can be attributed to the existence of broken and randomly dispersed fibers due to the weak adhesion forces between the carbon fibers and the epoxy matrix.

The use of carbon nanotubes (CNTs) as a reinforcing material in a polymer matrix has in-creased in various industries. In this study, the flexuralbehavior of CNT-modifiedepoxy/basalt (CNT/epoxy/basalt) composites is investigated. The effects of CNT modificationwith silane on the flexuralproperties of CNT/epoxy/basalt composites were also examined. Flexural tests were performed using epoxy/basalt, oxidized CNT/epoxy/basalt, and silanized CNT/epoxy/basalt multi-scale composites. After the flexuraltests, the fracture surfaces of the specimens were examined via scanning electron microscopy (SEM) to investigate the fracture mechanisms of the CNT/epoxy/basalt multi-scale composites with respect to the CNT modificatio process. The flexuralproperties of the epoxy/basalt composites were im-proved by the addition of CNTs. The flexuralmodulus and strength of the silane-treated CNT/epoxy/basalt multi-scale composites increased by approximately 54% and 34%, re-spectively, compared to those of epoxy/basalt composites. A SEM examination of the frac-ture surfaces revealed that the improvement in the flexuralproperties of the silane-treated CNT/epoxy/basalt multi-scale composites could be attributed to the improved dispersion of the CNTs in the epoxy.

본 논문은 에폭시 계열의 폴리머 콘크리트 교면포장 공법의 국내 적용 가능성을 검토하기 위하여 교면포장용 폴리설파이드 에폭시 재료에 대한 물리 역학적 특성을 평가하기 위하여 수행하였다. 강도특성을 평가하기 위하여 압축강도, 휨강도, 접착강도 시험을 수행하였으며 내구특성 평가를 위하여 염소이온침투시험, 동결융해저항성시험, 자외선영향 평가를 실시하였다. 시험결과 압축강도, 휨강도, 접착강도 등은 미국콘크리트협회에서 제시하는 기준을 만족하는 것으로 평가되었다. 그러나 다양한 시험온도에서의 강도 시험결과에서 에폭시 재료가 온도 의존성이 큰 것으로 나타나 향후 국내 적용시 이에 대한 고려가 필요할 것으로 판단된다. 휨강도 시험을 통한 처짐에 대한 추종성은 기존 아스팔트 교면포장에 비해 우수한 것으로 평가되었다. 또한 염소이온침투 저항성, 동결융해 저항성 등에 대해서도 우수한 성질을 가진 것으로 평가되었다. 에폭시 슬러리 혼합물에 대한 자외선 영향 평가에서는 강도 증가와 파괴시 변형률 감소가 나타났으나 자외선 노출 후에도 기존 아크릴계 폴리머 콘크리트보다 처짐에 대한 추종성이 양호한 것으로 평가되었다. 따라서 폴리설파이드 에폭시 재료가 교면포장 공법으로 사용하기에 적절한 물리적 특성을 가지고 있다고 판단된다.

This study aimed to investigate the influence of mesoporous carbons on the thermal insulation properties of epoxy/mesoporous carbon composites. The mesoporous carbon (CMK-3) was prepared by conventional templating method using SBA-15. The epoxy/mesoporous carbon composites were prepared by mixing the synthesized CMK-3 with diglycidylether of bisphenol A (DGEBA). As experimental results, the curing reactivities of the DGEBA/CMK-3 composites were found to decrease with the addition of the CMK-3. Also, the thermal conductivities of DGEBA/CMK-3 composites were found to decrease with increasing CMK-3 content. This could be interpreted in terms of the slow thermal diffusion rate resulting in pore volume existing in the gaps in the interfaces between the mesoporous carbon and the DGEBA matrix.

In this study, we experimented that how influence chain extension to waterborne urethane-epoxy hybrid resin for leather garment coatings. First of all, We had analyzed datas by FT-IR, SEM and machanical properties. By instruments analysis measurement we confirmed that synthesis of epoxy and hybrid resin. In this experiment we knew that polyurethane-epoxy hybrid resin have 5 grades of solvent resistance. Tensile strength measured in the polyurethane-epoxy resin(EDA 5.37g, 2.386 kgf/mm2) had the most strong strength.. Also polyurethane-epoxy hybrid resin had better result(EDA 5.37g. 37.4 mg. loss) than other hybrid resins. As hight proportion of EDA in hybid resin, we obtained low elongation and low flexibility. In this result, chain extension of waterborne polyurethane-epoxy hybrid resin showed that how effect in leather coating by ratio of EDA.

The relative viscosity was measured at different filler loadings for a cycloaliphatic epoxy resin and hexahydro-4-methylphthalic anhydride hardener system filled with micro/nano hybrid silica. Various empirical models were fitted to the experimental data and a fitting parameter such as critical filler fractions (φmax) was estimated. Among the models, the Zhang-Evans model gave the best fit to the viscosity data. For all the silica loadings used, ln (relative viscosity) varied linearly with filler loadings. Using the Zhang-Evans model and the linearity characteristics of the viscosity change, simple methods to predict the relative viscosity below φmax are presented in this work. The predicted viscosity values from the two methods at hybrid silica fractions of φ = 0.086 and 0.1506 were confirmed for a micro:nano = 1:1 hybrid filler. As a result, the difference between measured and predicted values was less than 11%, indicating that the proposed predicting methods are in good agreement with the experiment.

In this study, we experimented that how to synthesis waterborne urethane-epoxy hybrid resin for leather garment coatings. First of all, We had analyzed datas by FT-IR, SEM and TGA for the machanical properties. By instruments analysis measurement we confirmed that synthesis of urethane and epoxy. In this experiment we knew that polyurethane and urethane-epoxy hybrid resin have 4~5 grades of solvent resistance. Tensile strength measured in the urethane-epoxy resin(epoxy 12%, 2.033kgf/mm2) had the most strong strength than polyurethane(1.833 kgf/mm2) emulsion samples. Also urethane-epoxy hybrid resin had better result than polyurethane in acid resistance and abrasion test. As hight proportion of epoxy in hybid resin, we obtained low elongation and low flexibility. In this result, the mechanical properties of waterborne polyurethane-epoxy hybrid resin showed that how effect in leather coating by ratio of epoxy emulsion.

We prepared the amine epoxy adducts (AEA)/thin multiwalled carbon nanotubes (TWCNTs) composite particles using nonsolvent based methods including dry mechano-chemical bonding(MCB) process and supercritical fluid (SCF) process. The resulting TWCNTs/AEA composite particles have been used as curing agents for urethane modified bispheol A type epoxy resin. The thermal, thermomechanical properties of the epoxy resins cured with TWCNTs/AEA composite particles were measured by DMA and the dispersion of CNT was characterized by SEM. Because of high degree of CNT dispersion, thermal and mechanical properties of the epoxy resin cured with TWCNTs/AEA composite particles prepared by SCF process are better than those cured with mechano-chemically prepared TWCNTs/AEA composite particles.

Silicone surfactants are widely used in many industrial area because of its thermal stability and lower foaming property. But it has limitation to expand the application because of migration and bubble generation issues when it is mixed with organic surfactant. In this study, epoxy functionalized fluoro-silicone surfactant, perfluoro glycidoxypropyl polyether siloxane(PFGES), was synthesized using hydrosilylation reaction among perfluoro methyl hydrogen siloxane, allyl glycidyl ether, and allyl ployether in order to get lower surface tension, better thermal stability than conventional silicone surfactant, and reactivity with anhydride function.

In this work, the effect of co-carbon fillers on the electrical and mechanical properties of epoxy nanocomposites was investigated. The graphite nanosheets (GNs) and multi-walled carbon nanotubes (MWNTs) were used as co-carbon fillers. The results showed that the electrical conductivity of the epoxy nanocomposites showed a considerable increase upon an addition of MWNTs when GNs were fixed at 2 wt.%. This indicated that low content GNs formed the bulk conductive network and then MWNTs added were intercalated between the GN layers, resulted in the formation of additional conductive pathway. Furthermore, the flexural strength of the epoxy nanocomposites was enhanced with increasing the MWNT content. It was probably attributed to the flexible MWNTs compared with rigid GNs, resulted in the enhancement of the mechanical properties.

In this work, the effect of carbon nanofibers (CNFs) addition on physicochemical characteristics of CNFs-reinforced epoxy matrix nanocomposites was studied. Poly(amide imide) solutions in dimethylformamide were electrospun into webs consisting of 250±50 nm fibers which were used to produce CNFs through stabilization and carbonization processes. As a result, the CNFs with average diameter of 200±20 nm were obtained after carbonization process. The nanocomposites with CNFs showed an improvement of thermal stability parameters and fracture toughness factors, compared to those of the specimen without CNFs, which could be probably attributed to the higher specific surface area and larger aspect ratio of CNFs, resulting in improving the mechanical interlocking in the nanocomposites. Also, the applied external loading can effectively transfer to CNFs because strong interactions are resulted between the epoxy matrix and the CNFs.

The surface treatment effects of reinforcement filler were investigated based on the dynamic mechanical properties of mutiwalled carbon nanotubes (MWCNTs)/epoxy composites. The as-received MWCNTs(R-MWCNTs) were chemically modified by direct oxyfluorination method to improve the dispersibility and adhesiveness with epoxy resins in composite system. In order to investigate the induced functional groups on MWCNTs during oxyfluorination, X-ray photoelectron spectroscopy was used. The thermo-mechanical property of MWCNTs/epoxy composite was also measured based on effects of oxyfluorination treatment of MWCNTs. The storage modulus of MWCNTs/epoxy composite was enhanced about 1.27 times through oxyfluorination of MWCNTs fillers at 25℃. The storage modulus of oxyfluorinated MWCNTs (OF73-MWCNTs) reinforced epoxy composite was much higher than that of R-MWCNTs/epoxy composite. It revealed that oxygen content led to the efficient carbon-fluorine covalent bonding during oxyfluorination. These functional groups on surface modified MWCNTs induced by oxyfluorination strikingly made an important role for the reinforced epoxy composite.

Epoxy resin based encapsulants are widely used in semiconductor packaging applications. Epoxy resin based encapsulants are often subject to crack or delamination during the reliability test due to the thermal stress caused by high modulus nature of epoxy resins. Epoxy functional siloxanes are often added into epoxy resin to reduce the modulus so that the thermal stress can be reduced. Epoxy functional siloxanes, additives for reduced modulus, were synthesized and added into the curable epoxy resins. The modulus and the coefficient of thermal expansion (CTE) were also measured to investigate the thermal stress and to see whether the epoxy functional siloxane adversely affects the CTE or not. As a result, around 26% to 72% of thermal stress reduction was observed with no adverse effect on CTE.

BaTiO3/epoxy composites have been widely investigated as promising materials for embedded capacitors in printed circuit boards. It is generally known that the dielectric constant (K) of the BaTiO3/epoxy composites increases with improvement of the dispersion of BaTiO3 particles in the epoxy matrix that comes from adding surfactant. The influences of surfactant addition on the dielectric properties of the BaTiO3/epoxy composites are reported in the present study. The dielectric constant of the BaTiO3/epoxy composites is not significantly affected by the surfactant addition. However, the temperature coefficient of capacitance increases and the peel strength decreases as the amount of added surfactant increases. The influences of surfactant addition on the dielectric properties of the neat epoxy are also very similar to those of the BaTiO3/epoxy composites. The residual surfactant in the BaTiO3/epoxy composites affects the temperature coefficient of capacitance and the peel strength of the epoxy matrix, which in turn affects the temperature coefficient of capacitance and the peel strength of the BaTiO3/epoxy composites.

BaTiO3/epoxy composites can be applied as the dielectric materials for embedded capacitors. The effects of the degree of BaTiO3 particle agglomeration on the dielectric properties of BaTiO3/epoxy composites were investigated in the present study. The degree of particle agglomeration was controlled by the milling of the agglomerated particles. The size and content of the agglomerated BaTiO3 particles decreased with an increase in the milling time. The dielectric constants and polarizations of BaTiO3/epoxy composites abruptly decreased with the increase of the milling time. It was concluded that the dielectric constants and polarizations of BaTiO3/epoxy composites decreased as the degree of particle agglomeration decreased. The degree of agglomeration of BaTiO3 particles turned out to be a very influential factor on the dielectric properties of BaTiO3/epoxy composites.