The objectives of this study were the development of a synthesis technique for highly active nanosized ITO powder and the understanding of the reaction mechanisms of the ITO precursors. The precipitation and agglomeration phenomena in ITO and precursors are very sensitive to reaction temperature, pH, and coexisting ion species. Excessive ion and ions had a negative effect an synthesizing highly active powders. However, with a relevant stabilizing treatment the shape and size of ITO and precursors could be controlled and high density sintered products of ITO were obtained. By applying the reprecipitation process (or stabilization technique), highly active ITO and powders were synthesized. Sintering these powders at for 5 hours produced 97% dense ITO bodies.

ZnO nanopowders were synthesized by the sol-gel method using hydrazine reduction, and their gas responses to 6 gases (200 ppm of C2H5OH, CH3COCH3, H2, C3H8, 100 ppm of CO, and 5 ppm of NO2) were measured at 300 ~ 400˚C. The prepared ZnO nanopowders showed high gas responses to C2H5OH and CH3COCH3 at 400˚C. The sensing materials prepared at the compositions of [ZnCl2]:[N2H4]:[NaOH] = 1:1:1 and 1:2:2 showed particularly high gas responses (S = Ra/Rg, Ra : resistance in air, Rg : resistance in gas) to 200 ppm of C2H5OH(S = 102.8~160.7) and 200 ppm of CH3COCH3(S = 72.6~166.2), while they showed low gas responses to H2, C3H8, CO, and NO2. The reason for high sensitivity to these 2 gases was discussed in relation to the reaction mechanism, oxidation state, surface area, and particle morphology of the sensing materials.

For possible applications as luminescent materials for white-light emission using UV-LEDs, Ba2Mg(PO4)2:Eu2+ phosphors were prepared by a solid state reaction. The photoluminescence properties of the phosphor were investigated under ultraviolet ray (UV) excitation. The prepared phosphor powders were characterized to from a single phase of a monoclinic crystalline structure by a powder X-ray diffraction analysis. In the photoluminescence spectra, the Ba2Mg(PO4)2:Eu2+ phosphor showed an intense emission band centered at the 584 nm wavelength due to the f-d transition of the Eu2+ activator. The optimum concentration of Eu2+ activator in the Ba2Mg(PO4)2 host, indicating the maximum emission intensity under the excitation of a 395 nm wavelength, was 5 at%. In addition, it was confirmed that the Eu2+ ions are substituted at both Ba2+ sites in the Ba2Mg(PO4)2 crystal. On the other hand, the critical distance of energy transfer between Eu2+ ions in the Ba2Mg(PO4)2 host was evaluated to be approximately 19.3 A. With increasing temperature, the emission intensity of the Ba2Mg(PO4)2:Eu phosphor was considerably decreased and the central wavelength of the emission peak was shifted toward a short wavelength.

We have synthesized Eu3+-doped YVO4 phosphors by using a hydrothermal method and investigatedtheir luminescent properties. Aqueous solutions of Y2O3, V2O5, Eu2O3, and nitric acid with various pH valueswere used as the precursors. The crystallinity, surface condition, and emission characteristics were examinedusing XRD, FT-IR, and photo-excited spectrometer. Eu3+ incorporation followed by the efficient red emissionstrongly depends on the acidity of solution media. The emission intensity becomes stronger as the pH valuesincrease to 7 and then gradually decreases. This phenomenon might be related to the hydroxyl quenchingeffect, which is induced by surface bound OH- groups.

Silver particles were synthesized from silver nitrate by homogeneous precipitation and chemical reduction methods involving the intermediate silver cyanate. The obtained silver particles were characterized by XRD, SEM, TEM, and BET. Urea which could prevent the agglomeration of the reduced silver particles was used as a homogeneous precipitator. The spherical silver particles with average particle diameter of 100 nm were obtained under the optimum reaction conditions. The optimum synthetic conditions were found as follows: reaction temperature , reaction time 60 min, concentration of silver nitrate mol, urea mol, and sodium citrate mol. The phase of obtained silver particles was crystalline state and the silver particles were relatively dense, which had the surface area of .

The core-shell composite particles 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 core-shell structure of silicone dioxide/styrene in the presence of an anionic surfactant sodium lauryl sulfate (SLS) and polyoxyethylene alky lether sulfate (EU-S133D). We found that when SiO2 core/PSt shell polymerization was prepared on the surface SiO2 particle, to minimize the coagulation during the shell polymerization, the optimum conditions were at concentration of 2.56×10-2mole/L SLS. The structure of core-shell polymer was confirmed by measuring the thermal decomposition of polymer composite using thermogravimetric analyzer and morphology of core-shell polymer particles by transmission electron microscope (TEM).

Akt, a serine/threonine protein kinase as a viral oncogene, is a critical regulator of PI3K-mediated cell proliferation and survival. On translocation, Akt is phosphorylated and activated, ultimately resulting in stimulation of cell growth and survival. As a part of our program toward the novel Akt1 inhibitors with potent activity over PI3K signaling pathway, we found primary hit compound 2 with an IC50 value of 620μM from protein kinase focused library. Based on the structural features of 2, new 1,3,4-thiadiazole derivatives were designed by the introduction of aromatic and heteroaromatic moieties onto thiadiazole nucleus. In this work, a series of 1,3,4-thiadiazole derivatives 1a-1 were synthesized and evaluated for Akt1 inhibitory activity.

It is necessary to improve the esthetic and function in the patient with oral and maxillofacial bone defects. Synthetic bone substitute materials and anorganic bovine bone mineral(ABBM) have been used for clinical restoration. The purpose of this study was to observe the biocompatibility and bone formation of synthetic hydroxyapatite(SHA) and ABBM in hole of rabbit's tibia. After specimens with SHA and ABBM at 8 weeks were fixed in 10% neutral formalin solution, dehydrated, and embedded with spurr low viscosity, they were cut by 500um with slow diamond wheel saw and grinded up to 200um in thickness. These specimens were coated with carbon and examined with r efraction microscope for bone density. Refraction microscopic features of 8 weeks in synthetic HA showed network-like new bone forming trabecular pattern attached to resorbed HA. Less well calcified trabecular bone surrounding conglomerated HAs showed irregular arrangement of numerous osteocytes. There was not completely filled in defected area by new bone trabecular. New trabecular bone formation by ABBM was more prominent and completely compacted in defect hole at 8 weeks. It suggested that although bone formation activity of AMMB might be superior to that on synthetic HA, both group would be the good biocompatibility in this experiment.

SnO nanosheets were prepared at room temperature through a reaction between an aqueous solution of SnCl2, N2F4, and NaOH and were converted into SnO2 nanosheets without a morphological change. The SnO nanosheets were formed through a dissolution-recrystallization mechanism. Uniform and well-dispersed SnO nanosheets with the round-shape morphology were attained when the solution was treated by ultrasonic sound immediately after the addition of NaOH. The SnO2 nanosheets prepared by means of solution reduction under the ultrasonic treatment, and subsequent oxidation at 600˚C showed a high level of gas sensitivity to C2H5OH and CH3COCH3.

Pt-loaded carbon black for the catalyst of a PEM fuel cell was synthesized with different molar ratios of polyvinylpyrrolidone and H2PtCl6 solution to improve the dispersion of Pt nanoparticles on carbon black and decrease the size of Pt nanoparticles. From transmission electron microscopy results, Pt nanoparticles of a size of approximately 2 nm were highly dispersed when the polyvinylpyrrolidone concentration was 10mM. The electrochemical activity of the synthesized Pt/C catalysts was investigated by cyclic voltammetry, showing that the as-synthesized Pt-loaded carbon black catalyst had the best activity at a polyvinylpyrrolidone concentration of 10 mM.

섬유복합재료(Fiber Reinforced Polymer, FRP)는 경량성, 높은 설계기준강도, 비전기 비자성 및 내부식성의 특징 등으로 인하여 최근 건설분야에서 많은 연구가 진행되고 있다. 그 중 GFRP(Glass Fiber Reinforced Polymer)는 가격 경쟁성에서 우수하여 일반적으로 많이 사용되고 있다. 그러나 GFRP는 상대적으로 낮은 탄성계수를 가지고 있어 처짐이 과대하게 발생함으로 구조부재 단면으로서 활용되기 위해서는 단면이 커야하며, 설계시 사용하중에 의한 처짐 제한에 대한 검토를 실시해야 한다. 이에 본 연구에서는 언급된 기술적인 문제점을 해결하기 위하여 대형 단면의 적용이 가능하도록 모듈형식의 단면을 제안하였다. 그리고 FRP의 낮은 강성을 확보하군 위하여 콘크리트를 충진하는 새로운 FRP+콘크리트 합성 거더 형상을 개발하였다. 개발된 FRP)콘크리트 합성 거더의 전단지간비와 콘크리트 충진 여부에 따른 전단강도 및 처짐, 중립축 변화를 확인하고자 전단실험을 실시하였다.

Nano-sized tungsten disulfide () powders were synthesized by chemical vapor condensation (CVC) process using tungsten carbonyl () as precursor and vaporized pure sulfur. Prior to the synthesis of tungsten disulfide nanoparticles, the pure tungsten nanoparticles were produced by same route to define the optimum synthesis parameters, which were then successfully applied to synthesize tungsten disulfide. The influence of experimental parameters on the phase and chemical composition as well as mean size of the particles for the produced pure tungsten and tungsten disulfide nanoparticles, were investigated

Nano-sized TiO2-60 wt% SrO composite powders were synthesized by a sol-gel method using titanium isopropoxide and Sr(OH)2 · 8H2O as precursors. 3, -5, -7 wt%Ag spot-coated TiO2-60 wt% SrO composite powders were synthesized by a Ag electroless deposition method using TiO2-60 wt% SrO composite powders calcined at 1050˚C, which mainly exhibited the SrTiO3phase. However, a small number of rutile TiO2, Sr2TiO4 and SrO2 phases were also detected. In the Ag spot-coated powders synthesized by electroless deposition, nano-sized particles about 5-25 nm in diameter adhered to the TiO2-60 wt% SrO composite powders. The photocatalytic activity of Ag spot-coated TiO2-SrO and TiO2-SrO composite powders for degradation of phenol showed that all of TiO2-SrO composite powders were highly active under UV light irradiation. 7 wt%Ag spot-coated TiO2-60wt.%SrO composite powders had a relatively higher photocatalytic activity than did TiO2-SrO composite powders under visible light.

ZnO nanorod gas sensors were prepared by an ultrasound radiation method and their gas sensing properties were investigated for NO gas. For this procedure, 0.01, 0.005 and 0.001M of zinc nitrate hydrate [Zn(NO3)2 · 6H2O] and hexamethyleneteramine [C6H12N4] aqueous solutions were prepared and then the solution was irradiated with high intensity ultrasound for 1 h. The lengths of ZnO nanorods ranged from 200 nm to 500 nm with diameters ranging from 40 nm to 80 nm. The size of the ZnO nanorods could be controlled by the concentration of solution. The sensing characteristics of these nanostructures were investigated for three kinds of sensor. The properties of the sensors were influenced by the morphology of the nanorods.

The central role of tyrosine phosphorylation in cell proliferative signaling mechanisms provides another target for chemotherapy. The aim of this research is to develop new quinazoline derivatives that possess the inhibitory activity for depidermal growth factor receptor (EGFR) tyrosine kinase (TK) as protein kinase inhibitors. In this work, a series of new 4-anilino-6-guanidino-7-methoxyquinazoline derivatives (12a-l) were synthesized by the introduction of guanidine moiety at C-6 of quinazoline nucleus and evaluated for their EGFR TK inhibitory activities.

In this study, benzoxazolo carbocyanine is of industrial importance as green-sensitizing dye in the spectral sensitization. Sensitizing dye was prepared by the reaction of 2-methyl-3-sulfopropyl-4,5-benzoxazolium (inner salt) with triethyl orthobenzoate in the presence of triethylamine. The product was identified by using various analytical tools such as elemental analyzer, IR spectrophotometer, UV-Vis spectrophotometer, 1H-NMR spectrometer, TGA and DSC. The maximum absorption peak in methanol solvent was 507 nm. Therefore, it was concluded that benzoxazolo carbocyanine dye can be used as sensitizing dye for the spectral sensitization of photographic emulsion and color cosmetics.

The hydrosilylation is an addition reaction of Si-H bond to unsaturated double bonds, which provides a convenient mechanism to synthesize poly(dimethylsiloxane-co-methylsiloxane)copolymer having siloxy units in polymer backbone. In this study, Poly(dimethylsiloxane-co-methylsiloxane) copolymer was synthesized through the polymerization reaction of cyclopentasiloxane with poly(methyl-hydrogen) siloxane. Silicone-hydrogen functional group of the poly(dimethylsiloxane-co-methylsiloxane) copolymer was substituted to the alkyl groups by hydrosilylation. And their structure was analyzed with FT-IR, H-NMR and GPC instruments, respectively. Surface tension of the synthetic compounds is increased from 22dyne/cm to 25dyne/cm according to increase additional EO moles. The cmc which was evaluated by surface tension was ranged 10-5 to 10-4mol/L and it was decreased according to increase of dimethyl siloxyl content. HLB number of these surfactants was evaluated 9.5 to 11.5 range. These silicone surfactants is applied to self-emulsifier defoamer and personal care products as surface tension depressant, emulsifier, foam control agent.