주사슬에 실리콘을 포함하는 단량체를 단계별로 합성을 하였고, 합성된 단량체와 테트라아민기를 갖는3,3-diaminobenzidine과의 축합중합 방법을 통하여 두 가지 새로운 중합체 PBI 1, PBI 2를 합성하였다.합성된 중합체들의 구조분석은 IR, 1H-NMR 측정을 통해서 확인하였고, 분자량 분포를 알아보기위해서GPC를 측정한 결과 다분산지수가 1.55로 측정 되었다. PBI의 물리적, 열적 특성을 알아보기 위해서 용해도 조사, 점도 측정 그리고 TGA 측정을 하였다. 그 결과 중합체가 DMAc, DMSO, NMP, DMF 등의 극성 유기용매에 잘 용해되었으며, 열안정성은 초기분해온도가 368℃이고, 800℃에서 잔존질량이 57%로 열적 안정성이 우수한 고분자임을 확인하였다.

우수한 열안정성과 낮은 구동전압을 가지면서 수명이 길고 발광 효율이 우수한 유기 EL 고분자인 PPV계열의 새로운 MEH-PPV[1,4-비스(브로모메틸)-2-(2-에틸헥실옥시)-5-메톡시벤젠] 주사슬에 2,5-비스(4-(브로모메틸)페닐)-1,3,4-옥사디아졸과 2,7-디브로모-9,9-디옥틸-9H-플루오렌을 첨가시켜 공중합하여MEH-O-DPPV 공중합체를 합성하였으며, 합성된 MEH-O-DPPV 공중합체가 기존의 MEH-PPV 동종중합체과 열적 안정성, 분광학적 특성 및 발광 특성을 비교 분석하였다. 합성된 MEH-O-DPPV 공중합체와 PMMA을 1:50중량비로 용액 제조 후 나노섬유를 만들어 광학 현미경으로 관찰하였다.

이 논문에서는 기존의 CFFT(Concrete Filled FRP Tube) 복합재 말뚝의 휨강성을 확보하기 위한 새로운 복합재 말뚝 형식을 제안하였다. 기존의 CFFT 복합재 말뚝은 필라멘트와인딩 공정으로 제작한 FRP를 사용하기 때문에, 압축력 이 편심재하될 경우 휨거동에 대한 안전성을 확보하기 위해 철근 등 별도의 보강재를 필요로 한다. 이 연구에서는 별도의 보강재 없이 휨거동에 대한 저항성을 확보하기 위하여 펄트루젼 방식으로 제작된 FRP를 CFFT 외부에 원주 방향으로 부착시킨 FRP-콘크리트 합성말뚝(Hybrid CFFT, HCFFT)을 제안하였다. 이 논문은 HCFFT의 구조적 거동 을 검토하기 위한 연구의 일부로서, HCFFT에 사용되는 필라멘트와인딩 FRP의 역학적 특성을 알기 위한 실험을 실 시하였다. 또한, 기존 연구 결과를 참조하여 HCFFT의 압축강도를 추정하였으며, 유한요소해석을 통해 얻은 결과와 비교분석하였다.

마이크로파를 열원으로 이용하는 화학반응은 어려운 반응을 활성화시킬 수 있고 반응시간과 속도를 가속화하여 고수득율 및 높은 분자량을 얻는 고분자를 합성하는데 유용하게 쓰일 수 있다. 본 연구에서는마이크로파를 이용하여 Diels-Alder 반응을 실시하고 열적으로 안정한 측사슬계 2차 비선형광학고분자를 합성하였다. 일반적인 수열반응을 통해 얻어진 고분자와 물리적, 열적, 광학적 특성을 비교 분석하였으며 마이크로파 가열을 활성화하기 위해 용매를 달리하고 이온성액제를 첨가하여 반응을 조절하였다. PAMID시리즈의 다양한 고분자를 합성하였으며 이중에서 PAMID-M2는 10분간 120W의 전력을 사용하여 얻어졌으며 이 때 사용한 용매는 이온성액제가 소량 첨가된 trichloroethane을 사용하였다. 얻어진PAMID-M2의 무게평균 분자량은 18,300이었으며 분포도는 1.3이었고 높은 유리전이온도 (123oC)를 나타냈다.

ZnO nanostructures were grown on an Au seed layer by a hydrothermal method. The Au seed layer was deposited by ion sputter on a Si (100) substrate, and then the ZnO nanostructures were grown with different precursor concentrations ranging from 0.01 M to 0.3M at 150˚C and different growth temperatures ranging from 100˚C to 250˚C with 0.3 M of precursor concentration. FE-SEM (field-emission scanning electron microscopy), XRD (X-ray diffraction), and PL (photoluminescence) were carried out to investigate the structural and optical properties of the ZnO nanostructures. The different morphologies are shown with different growth conditions by FE-SEM images. The density of the ZnO nanostructures changed significantly as the growth conditions changed. The density increased as the precursor concentration increased. The ZnO nanostructures are barely grown at 100˚C and the ZnO nanostructure grown at 150˚C has the highest density. The XRD pattern shows the ZnO (100), ZnO (002), ZnO (101) peaks, which indicated the ZnO structure has a wurtzite structure. The higher intensity and lower FWHM (full width at half maximum) of the ZnO peaks were observed at a growth temperature of 150˚C, which indicated higher crystal quality. A near band edge emission (NBE) and a deep level emission (DLE) were observed at the PL spectra and the intensity of the DLE increased as the density of the ZnO nanostructures increased.

The ultrafine titanium carbonitride () particles below 100 nm in mean size, including various carbon and nitrogen contents (x=0.55~0.9, y=0.1~0.5), were successfully synthesized by new Mg-thermal reduction process. Nanostructured sub-stoichiometric titanium carbide () particles were initially produced by the magnesium reduction of gaseous at and post heat treatments in vacuum were performed for 2 hrs to remove residual magnesium and magnesium chloride mixed with . Finally, well C/N-controled phases were successfully produced by nitrification heat treatment under normal gas atmosphere at for 2 hrs. The values of purity, mean particle size and oxygen content of produced particles were about 99.3%, 100 nm and 0.2 wt.%, respectively.

In this study, we successfully synthesized a nano-sized lanthanum-modified lead-titanate (PLT) powder with a perovskite structure using a high-energy mechanochemical process (MCP). In addition, the sintering behavior of synthesized PLT nanopowder was investigated and the sintering temperature that can make the full dense PLT specimen decreased to below by using powder as sintering agent. The pure PLT phase of perovskite structure was formed after MCP was conducted for 4 h and the average size of the particles was approximately 20 nm. After sintered at 1050 and , the relative density of PLT was about 93.84 and 95.78%, respectively. The density of PLT increased with adding and the specimen with the relative densitiy over 96% were fabricated below when 2 wt% of was added.

Nano-sized BaNd2Ti5O14 powders were prepared by the spray pyrolysis process. Sucrose used as the organic additive enabled the formation of nano-sized BaNd2Ti5O14 powders. The powders prepared from the spray solution without sucrose had a spherical shape, dense structure and micron size before and after calcination. However, the precursor powders prepared from the spray solution with sucrose had a large size, and hollow and porous morphology. The precursor powders had an amorphous crystal structure because of the short residence time of the powders inside the hot wall reactor. The complete decomposition of sucrose did not occur inside the hot wall reactor. Therefore, the precursor powders obtained from the spray solution with sucrose of 0.5M had a carbon content of 39.2wt.%. The powders obtained from the spray solution with sucrose of 0.5M had a slightly aggregated structure of nano-sized primary powders of BaNd2Ti5O14 crystalline phase after calcination at 1000˚C. The calcined powders turned into nano-sized BaNd2Ti5O14 powders after milling. The mean size of the BaNd2Ti5O14 powders was 125 nm.

Silicone dioxide absorbed polyoxyethylene alkylether sulfate (EU-S75D) surfactant was prepared. The core-shell composite of inorganic/organic were polymerized by using styrene(St) as a shell monomer and potassium persulfate(KPS) as an initiator. We studied the effect of surfactants on the core-shell structure of silicone dioxide/styrene in the presence of an anionic surfactant lauryl sulfate(SLS). The structure of core-shell polymer were investigated by measuring to the thermal decomposition of polymer composite using thermogravimetric analyzer(TGA) and morphology of latex by scanning electron microscope(SEM).

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.

Titanium dioxide particles are used as photocatalysts, sensors, adsorbents and catalyst. Core-shell polymers of inorganic/organic pair, which have both core and shell component, were synthesized by sequential emulsion polymerization using Acrylate as a shell monomer and potassium persulfate (KPS) as an initiator. We found that when Acrylate core prepared by adding 0.5~2.0 wt% EU-S133D, Titanium dioxide / Acrylate core-shell polymerization was carried out on the surface of Titanium dioxide particle without forming the new Titanium dioxide particle during acrylate shell polymerized in the inorganic/organic core-shell polymer preparation. The structure of core-shell polymer were investigated by measuring to the thermal decomposition of polymer composite using thermogravimetric analyzer(TGA) and morphology of latex by scanning electron microscope(SEM).

Melanoma is the most aggressive form of skin cancer and is the fastest growing type of cancer in the United States. We report here the synthesis of a novel series of quinazolinylmethoxybenzene derivatives 1a-c and their antiproliferative activities against A375 human melanoma cell line. Among them, urea compound 1a (IC50 = 4.8 μM) having 4-chloro-3-trifluoromethylphenyl moiety showed superior antiproliferative activity to Sorafenib (IC50 = 5.5 μM) as a reference compound. These results will helpful for designing structure of a therapeutic agent for the treatment of melanoma.

8 mol% Y-doped powder was synthesized by Pechini method from titanium isopropoxide, strontium nitrate, yttrium nitrate, citric acid and ethylene glycol. A pyrochlore phase-free perovskite powder was obtained by calcining a polymeric resin, which was prepared from a precursor solution, at in an air atmosphere. Low temperature calcination could lead to a fine-grained microstructure. In the case of a solid-state reaction, an extended heat-treatment at high temperature in a reduced atmosphere needed to obtain a single phase perovskite .

Si nanowire/multiwalled carbon nanotube nanocomposite arrays were synthesized. Vertically aligned Si nanowire arrays were fabricated by Ag nanodendrite-assisted wet chemical etching of n-type wafers using HF/AgNO3 solution. The composite structure was synthesized by formation of a sheath of carbon multilayers on a Si nanowire template surface through a thermal CVD process under various conditions. The results of Raman spectroscopy, scanning electron microscopy, and high resolution transmission electron microcopy demonstrate that the obtained nanocomposite has a Si nanowire core/carbon nanotube shell structure. The remarkable feature of the proposed method is that the vertically aligned Si nanowire was encapsulated with a multiwalled carbon nanotube without metal catalysts, which is important for nanodevice fabrication. It can be expected that the introduction of Si nanowires into multiwalled carbon nanotubes may significantly alter their electronic and mechanical properties, and may even result in some unexpected material properties. The proposed method possesses great potential for fabricating other semiconductor/CNT nanocomposites.

Different types magnesium hydroxide groups have been obtained using the hydrothermal precipitation technique from magnesium sulfate and calcium carbonate solution. The Mg atom coordinated around O atom of SO42- in another layer to form a multi-layer structure crystal. The influence of synthesis parameters on the morphological characteristics and size of magnesium hydroxide groups precipitated in aqueous were investigated such as different of additive and pH. Magnesium hydroxide groups were decomposed gradually and converted finally to MgO particles after heated in air temperature up to 1050℃. The particle size and it's distribution morphology, crystal phase and thermal behavior of the samples were characterized through XRD, SEM, EDS, and TG/DTA.

Poly propylene carbonate (PPC)와 cloisite 20B (PPC/C-20B)을 solution method를 통하여 합성하였고, 이를 통해 합성된 나노 조성물의 morphology, 열적 특성, 수분 흡수의 특성을 평가하였다. 나노 조성물의 구조는 X-ray diffraction (XRD) 로 확인하였고, 열적 특성은 thermal gravimetric analysis (TGA)와 differential scanning calorimetric (DSC)를 이용해 분석하였다. TGA와 DSC의 결과를 통해 나노 조성물은 기존의 PPC에 비해 높은 열적 안정성을 가짐을 확인할 수 있었다. DSC측정에서 5 wt%의 clay를 포함한 nanohybrid의 유리전이온도는 순수한 PPC의 21℃에서 30℃로 9℃ 증가하였고, TGA 측정을 통해 확인한 열분해온도(Td50%)는 순수 PPC에 비해 23℃가 높아졌음을 확인하였다. 또한 PPC 나노 조성물의 수분 흡수량은 기존의 PPC에 비해 상당히 감소하였다. 이는 clay의 PPC matrix 구조 내에 존재함으로 인해 수분 흡수를 감소시킨 것으로 해석할 수 있다. 수분 흡수는 코팅 막의 분해를 유발하고 물리적, 기계적 성능에 영향을 미친다. 따라서 나노 조성물로 인한 PPC의 열적 안정성, 수분흡수도 향상은 PPC의 사용과 실제 공정에 중요한 변수로 작용할 수 있다.